Why IVF Fails: Understanding Where in the Process
IVF failure happens at different points in the cycle and identifying where it failed is the first step to understanding why. Your clinic’s embryology report and cycle records should tell you which of the following scenarios occurred:
| Failure point | What happened | Most likely cause |
|---|
| Poor stimulation response | Few eggs retrieved (fewer than 3) | Low AMH, wrong protocol, poor ovarian reserve |
| No eggs retrieved | Follicles present but no eggs | Empty follicle syndrome, trigger failure, lab issue |
| Fertilisation failure | Eggs retrieved but none fertilised | Sperm quality, egg quality, ICSI needed but not used |
| Embryo arrest (Day 2–3) | Embryos stopped developing before transfer | Embryo chromosomal abnormality, lab quality, sperm DNA |
| No blastocysts formed | Embryos reached Day 3 but not Day 5 | Embryo quality, laboratory environment |
| Implantation failure | Good embryo transferred, no pregnancy | Endometrial receptivity, uterine pathology, immune factors |
| Biochemical pregnancy | Positive beta HCG, then negative | Early embryo chromosomal abnormality, inadequate luteal support |
| Clinical miscarriage | Heartbeat seen, then lost | Chromosomal abnormality, thrombophilia, uterine issue |
The most important question after a failed cycle:
Ask your clinic exactly which failure point occurred. The answer changes your investigation and your next protocol completely.
12 Reasons IVF Fails: Cause, Investigation, and Solution
Reason 1: Poor Egg Quality (Most Common – Especially Over 35)
What happens: The eggs retrieved do not fertilise well, produce poor-quality embryos, or embryos arrest early. Even when blastocysts form, they may be chromosomally abnormal unable to implant or sustaining a pregnancy.
Why it happens: Egg quality declines with age because the spindle apparatus responsible for correct chromosomal separation becomes less efficient. By age 35, chromosomal abnormality rates in eggs begin rising significantly. By age 42, over 70% of eggs may carry chromosomal errors. Non-age causes include endometriosis, smoking, nutritional deficiencies, and low antioxidant status.
Learn : endometriosis treatment
Investigation:
- Detailed embryology report review fragmentation rates, cell symmetry, blastulation rate
- PGT-A (preimplantation genetic testing) on embryos in the next cycle definitive answer on chromosomal status
- Sperm DNA fragmentation test high DNA fragmentation in sperm contributes to poor embryo quality even when the egg is healthy
Solution:
- CoQ10 (600mg ubiquinol daily) for 60–90 days before the next cycle improves mitochondrial function in oocytes
- DHEA (75mg daily, 8–12 weeks pre-cycle) improves ovarian androgen environment, improves egg quality in poor responders
- Protocol change different stimulation approach (e.g., mini-IVF, DuoStim)
- PGT-A in next cycle only chromosomally normal embryos transferred
- If egg quality cannot be improved: honest discussion of donor egg IVF
Reason 2: Wrong Stimulation Protocol
What happens: The stimulation produces too few eggs (poor responder) or too many (risk of OHSS) both outcomes compromise cycle success.
Why it happens: No stimulation protocol works equally for all patients. Women with PCOS need low-dose gentle stimulation; women with low AMH need high-dose or DuoStim protocols; women with previous OHSS need antagonist protocols with GnRH trigger. Using a generic protocol is the most common clinic-side cause of preventable IVF failure.
Investigation:
- Full review of stimulation monitoring records: Day 6, 8, 10 follicle counts and oestradiol levels
- AMH and AFC (antral follicle count) re-assessment if more than 6 months old
- Review of trigger injection used and timing
Solution:
- Complete stimulation protocol redesign based on individual profile
- For poor responders: DuoStim (two retrieval cycles in one month), mini-IVF, or adjuvant DHEA
- For PCOS patients: letrozole co-treatment, GnRH antagonist protocol, GnRH agonist trigger to prevent OHSS
- Adjust trigger timing: some patients respond better to dual trigger (HCG + GnRH agonist)
Reason 3: Endometrial (Uterine Lining) Failure – Implantation Failure
What happens: The embryo fails to implant despite good quality. The most common clinic-side missed cause of recurrent IVF failure.
Why it happens: The uterine lining may be too thin (below 7mm), have absent trilaminar pattern, have reduced blood flow, contain an undiagnosed polyp, fibroid, or adhesion or the lining may be structurally normal but functionally unreceptive (displaced implantation window).
Investigation:
- 3D saline infusion sonography (SIS) detects polyps, fibroids, adhesions not visible on standard ultrasound
- Hysteroscopy direct visualisation of the uterine cavity; gold standard for cavity evaluation
- Uterine artery Doppler assesses blood flow to the endometrium
- ERA test (Endometrial Receptivity Analysis) checks if the implantation window is at the expected time
- ALICE test (Analysis of Infectious Chronic Endometritis) checks for chronic endometrial infection
- Endometrial TB screen (MGIT culture + PCR) critical in Indian patients: up to 15% of infertile Indian women have endometrial TB causing silent damage to the lining
Solution:
- Polyps, fibroids, adhesions → hysteroscopic treatment before next cycle
- Thin lining → vaginal sildenafil, low-dose aspirin, PRP intrauterine infusion, G-CSF infusion
- ERA-diagnosed displaced window → personalised embryo transfer timing (pET)
- Chronic endometritis → antibiotic treatment course before next cycle
- Endometrial TB → complete anti-TB treatment course (6–9 months); re-evaluate lining after
Read the full endometrial thickness guide →
Reason 4: Embryo Chromosomal Abnormality (Aneuploidy)
What happens: The embryo appears morphologically normal (good grade on Day 5) but carries chromosomal errors (wrong number of chromosomes). It fails to implant, or implants briefly (biochemical pregnancy) and then fails.
Why it happens: Chromosomal errors in embryos are the single most common cause of IVF failure and early miscarriage. Rates increase sharply with age: approximately 25% of embryos are aneuploid at age 30; by age 42, over 75% may be aneuploid. Even in younger women, 15–25% of morphologically good embryos carry chromosomal errors invisible to the embryologist’s eye.
Investigation:
- PGT-A (Preimplantation Genetic Testing for Aneuploidy) on embryos in the next cycle
- Parental karyotyping — if PGT-A shows repeated patterns of specific errors, parental chromosome structural variations may be responsible
Solution:
- PGT-A in the next cycle — transfer only chromosomally normal (euploid) embryos
- Significantly improves implantation rate per transfer for patients over 35, with recurrent failure, or with recurrent miscarriage
- In cases of structural chromosomal rearrangements in parents: PGT-SR (structural rearrangement testing)
Reason 5: Sperm DNA Fragmentation
What happens: The sperm appears normal on semen analysis (count, motility, morphology all normal) but carries DNA damage that impairs embryo development leading to fertilisation failure, early embryo arrest, or recurrent implantation failure.
Why it happens: Sperm DNA damage is caused by oxidative stress, elevated testicular temperature (varicocele, laptop use, tight clothing), infection, smoking, alcohol, and age. Standard semen analysis does not detect DNA fragmentation a patient can have a “normal” semen analysis and high DNA fragmentation simultaneously.
Investigation:
- Sperm DNA Fragmentation Index (DFI) test – DFI above 15–25% is associated with significantly impaired IVF outcomes
- Testicular sperm extraction (TESE) assessment in cases of very high fragmentation, testicular sperm (which have less DNA damage than ejaculated sperm) may be used for ICSI
Solution:
- Antioxidant supplementation: Vitamin C (1g/day), Vitamin E (400 IU/day), CoQ10 (300mg/day), zinc, selenium 90 days minimum
- Varicocele treatment if present
- If DFI remains high despite treatment: TESE-ICSI using testicular sperm
Reason 6: Implantation Window Displacement (ERA – Endometrial Receptivity Analysis)
What happens: The embryo is transferred on Day 5 after progesterone start (standard timing), but the patient’s personal implantation window is shifted opening earlier or later than expected. A perfectly healthy embryo is transferred into a lining that is not yet (or no longer) receptive.
Why it happens: The endometrial window of implantation is genetically variable. Approximately 30–40% of patients with recurrent implantation failure have a displaced window but it is invisible on standard ultrasound and goes undetected without ERA testing.
Investigation:
- ERA test (Endometrial Receptivity Analysis) an endometrial biopsy is taken at standard transfer timing, analysed by RNA sequencing. Result: “Receptive” (transfer at standard time) or “Non-receptive” with exact recommended transfer time adjustment
Solution:
- Personalised Embryo Transfer (pET) transfer timed to the patient’s specific window based on ERA result
- Studies show pET in ERA-confirmed displaced-window patients improves implantation rates significantly compared to standard timing
Reason 7: Uterine Structural Abnormalities (Fibroids, Polyps, Septum, Adhesions)
What happens: A physical obstruction or distortion of the uterine cavity prevents embryo implantation or disrupts early development.
Why it happens: Submucosal fibroids (fibroids that protrude into the cavity) and endometrial polyps physically block implantation. Uterine septum (a tissue band dividing the cavity) creates a poorly vascularised surface the embryo cannot attach to. Intrauterine adhesions (Asherman syndrome from prior D&C, surgery, or TB) restrict available implantation surface.
Investigation:
- 3D saline infusion sonography (SIS) sensitive for polyps and small fibroids
- Hysteroscopy gold standard; allows simultaneous diagnosis and treatment
- MRI for adenomyosis assessment and fibroid location mapping
Solution:
- Hysteroscopic polypectomy polyp removal in an outpatient procedure
- Hysteroscopic myomectomy submucosal fibroid removal
- Hysteroscopic adhesiolysis adhesion removal for Asherman syndrome
- Septal resection for uterine septum
- All structural corrections should be confirmed healed before the next IVF cycle (typically 2–3 months post-surgery)
Reason 8: Immunological Factors – NK Cells and Autoimmune Rejection
What happens: The immune system, which would normally tolerate the embryo, mounts a rejection response. The embryo fails to implant or is rejected shortly after implantation begins.
Why it happens: Uterine Natural Killer (uNK) cells play a role in early implantation — but when present in excess, or when the immune response is dysregulated, they can reject the embryo. Antiphospholipid syndrome (APS), elevated NK cell activity, and HLA compatibility issues between partners are the most studied immune causes of recurrent IVF failure.
Investigation:
- Uterine NK cell testing — endometrial biopsy analysed for NK cell density
- Antiphospholipid antibody panel — lupus anticoagulant, anticardiolipin, anti-β2 glycoprotein-I
- Thrombophilia screen — Factor V Leiden, prothrombin mutation, protein C, protein S, antithrombin III
- Thyroid autoantibodies (anti-TPO, anti-Tg) — thyroid autoimmunity is associated with implantation failure
Solution:
- Elevated NK cells → intralipid infusion, prednisolone, G-CSF uterine infusion
- APS → low-molecular-weight heparin (LMWH) + low-dose aspirin throughout cycle
- Thrombophilia → LMWH from embryo transfer through first trimester
- Thyroid autoimmunity → levothyroxine optimisation, TSH below 2.5 before transfer
Reason 9: Hormonal Imbalance – Thyroid, Prolactin, Progesterone
What happens: Hormonal imbalances disrupt follicle development, endometrial preparation, or luteal support — causing poor egg quality, thin lining, or early pregnancy loss.
Why it happens:
- Hypothyroidism (TSH above 2.5 mIU/L during IVF) impairs follicle development and implantation
- Elevated prolactin interferes with ovulation and luteal phase function
- Inadequate progesterone support during the luteal phase prevents endometrial transformation and early pregnancy maintenance
- Premature progesterone rise during stimulation (above 1.5 ng/mL on trigger day) reduces fresh transfer success by impairing endometrial receptivity
Learn Here: PCOS and fertility
Investigation:
- TSH, free T4 — target TSH below 2.5 before IVF; below 2.0 ideally
- Prolactin — check and treat if elevated
- Progesterone level on trigger day — if elevated, consider elective freeze-all and FET
- Luteal phase progesterone monitoring — 7 days post-transfer to confirm adequate support
Solution:
- Hypothyroidism → levothyroxine dose optimisation minimum 6 weeks before cycle start
- Elevated prolactin → cabergoline treatment, re-test before starting
- Premature progesterone rise → freeze-all strategy; transfer in subsequent FET cycle when lining is optimally prepared
- Inadequate luteal support → increase progesterone dose or switch route (vaginal to intramuscular)
Read more : beta HCG after embryo transfer
Reason 10: Male Factor – Severe or Undetected Sperm Problems
What happens: Fertilisation fails or embryo quality is poor due to sperm-side factors that were not adequately identified or addressed before the IVF cycle.
Why it happens: Standard IVF (without ICSI) can fail if sperm cannot penetrate the egg’s zona pellucida. Severe morphology defects, low motility, or high DNA fragmentation can impair fertilisation or embryo development even when ICSI is used.
Learn : TESA for azoospermia
Investigation:
- Repeat semen analysis — ideally at the same lab with Kruger strict criteria for morphology
- Sperm DNA fragmentation index (DFI)
- Sperm chromatin structure assay (SCSA)
- If azoospermia: TESA / micro-TESE assessment
Solution:
- If ICSI was not used: ICSI in next cycle for all fertilisation
- High DFI: antioxidant treatment + consider TESE-ICSI
- Azoospermia: surgical sperm retrieval (TESA/PESA/micro-TESE) — Janisthaa IVF offers all procedures
- Morphology: IMSI (intracytoplasmic morphologically selected sperm injection) — selects best sperm under 6,000x magnification
Reason 11: Poor Ovarian Response (Low AMH / Diminished Reserve)
What happens: The ovaries produce very few follicles during stimulation (fewer than 3–4), reducing the number of embryos available and increasing the chance that none reach the blastocyst stage.
Why it happens: Low AMH (below 1.0 ng/mL) indicates a reduced pool of antral follicles available to recruit. Even with maximum stimulation, the number of eggs retrieved may be insufficient for a successful cycle.
Investigation:
- Re-assess AMH and AFC — has AMH fallen further since last test?
- Review stimulation monitoring in detail — at what follicle size were eggs triggered? Could trigger timing be optimised?
Solution:
- DHEA pre-treatment (75mg daily, 8–12 weeks) before next cycle
- DuoStim protocol — two stimulation phases per cycle, doubling egg collection
- Embryo banking — 2–3 stimulation cycles, freeze all embryos, then transfer best blastocyst
- Mini-IVF — fewer drugs, focus on quality over quantity
- Donor egg IVF if own-egg IVF consistently yields no usable blastocysts
Read the complete low AMH guide →
Reason 12: Laboratory Quality Issues
What happens: Embryos that should develop to blastocyst stage fail to do so — not because of the patient’s biology but because of the laboratory environment in which they are cultured.
Why it happens: IVF embryo culture is extraordinarily sensitive to environmental conditions. Temperature fluctuations outside 0.1°C of target, CO₂ levels outside narrow parameters, volatile organic compounds (VOCs) in lab air, incubator door openings, and embryologist handling technique all directly affect blastocyst development rates. Poor laboratory conditions cause embryo arrest that looks identical to poor egg or sperm quality.
Signs this may be the issue:
- Your embryos consistently arrest at the same developmental stage (e.g., always arrest Day 2–3)
- Your embryo quality was reportedly “good” at Day 3 but none reached blastocyst
- You are younger than 35 with good AMH and semen analysis but consistently produce no blastocysts
Investigation:
- Request a detailed embryology report from your previous clinic — ask for: fertilisation rate, cleavage rates Day 2 and 3, blastulation rate Day 5 and 6, grading of each blastocyst
- Compare against published benchmarks: a good laboratory should produce Day 5 blastocysts in 40–60% of fertilised eggs
Solution:
- Change clinic — specifically choose a clinic whose laboratory benchmarks and blastulation rates are documented
- At Janisthaa IVF: our laboratory maintains continuous temperature and gas monitoring, HEPA and VOC filtration, and embryologist continuity. Blastulation rates are tracked per embryologist and per patient cohort.
Advanced Investigations for Recurrent IVF Failure
If you have had 2 or more IVF failures with good-quality embryos, the standard investigations may not be enough. The following advanced workup is recommended at Janisthaa IVF for all patients with recurrent implantation failure (RIF):
Recurrent IVF Failure Investigation Panel at Janisthaa IVF
| Investigation | What it finds | Who it is for |
|---|
| ERA (Endometrial Receptivity Analysis) | Displaced implantation window — affects 30–40% of RIF patients | All patients with 2+ failed transfers of good embryos |
| ALICE (Chronic Endometritis Panel) | Bacterial infection of the endometrium causing implantation failure | All RIF patients with prior uterine instrumentation |
| Endometrial TB screen (MGIT + PCR) | Tuberculosis of the endometrium — 10–15% of Indian infertile women | India-specific — all unexplained RIF cases |
| Sperm DNA Fragmentation Index (DFI) | DNA damage in sperm not detected by standard semen analysis | All male partners with unexplained fertilisation or embryo failure |
| Uterine NK cell biopsy | Elevated natural killer cells causing embryo rejection | Patients with implantation failure and no structural cause |
| Antiphospholipid antibody panel | Autoimmune clotting disorder causing early pregnancy loss | Recurrent biochemical pregnancies or miscarriages |
| Full thrombophilia screen | Inherited clotting disorders — impair placental blood flow | Family history of clotting, recurrent loss |
| PGT-A on embryos (next cycle) | Chromosomal status of each embryo | All patients over 38, all with 2+ unexplained failures |
| 3D hysteroscopy | Structural uterine cavity evaluation | All RIF patients — before every new cycle |
| Parental karyotype | Chromosomal structural rearrangements in parents | If PGT-A shows specific patterns of abnormality |
Cumulative Success After IVF Failure: The Numbers You Need
The single most important piece of information for a patient after a failed IVF cycle is: what are my realistic chances next time?
Cumulative IVF Success Rate by Number of Cycles
| Cycles attempted | Cumulative live birth rate (women under 38) | Key variable |
|---|
| After 1 cycle | 35–50% | Depends on age and embryo quality |
| After 2 cycles | 55–65% | Increases significantly — protocol learnings applied |
| After 3 cycles | 65–80% | Most success occurs within 3 cycles for good-prognosis patients |
| After 4–6 cycles | 70–85% | Diminishing returns after cycle 4 — reassess with advanced investigations |
Success Rate After Specific Protocol Changes
| Protocol change | Improvement in success |
|---|
| ERA-guided pET after standard timing failure | 20–30% improvement in implantation rate |
| PGT-A after recurrent embryo failure | Reduces miscarriage rate by 50%; improves per-transfer success |
| TESE-ICSI after high sperm DFI | Significantly improves embryo quality and blastulation rate |
| Hysteroscopy + treatment before FET | 15–25% improvement in implantation after structural correction |
| Endometrial TB treatment before next cycle | Near-complete recovery in some patients — essential to identify |
Your Step by Step Action Plan After a Failed IVF Cycle
Step 1 – Request a formal debrief from your clinic (immediately)
Every failed IVF cycle should trigger a structured medical review. Request a meeting within 2–4 weeks that covers:
- The complete embryology report: how many eggs, how many fertilised, how many reached which stage
- The stimulation monitoring records: follicle growth curve, oestradiol levels, endometrial measurements
- What the doctor believes is the primary failure cause
- What protocol changes are recommended for the next cycle
If your clinic cannot provide this review or provides only generic explanations without specific data, that is a clinical red flag.
Step 2 – Get your complete cycle records
Request copies of:
- Stimulation protocol and medication doses
- All monitoring scan reports
- All blood test results from the cycle
- Embryology report (fertilisation rates, cleavage rates, blastocyst grades)
- Transfer report (embryo grade, endometrial measurement, transfer notes)
- Beta HCG results
You are entitled to all of these. Bring them to any second opinion appointment.
Step 3 – Allow adequate recovery time
Most specialists recommend waiting at least one full natural menstrual cycle (4–6 weeks) before starting investigations or a new cycle. This gives the body time to recover from stimulation hormones and reduces OHSS risk in subsequent cycles.
Use this time productively: start CoQ10 and vitamin D supplementation, optimise BMI if needed, stop smoking, and book investigations.
Step 4 – Complete the recommended investigations before the next cycle
Based on your failure pattern (see Section 2), complete the relevant investigations. Do not start a new cycle with the same protocol before results are back and reviewed.
Step 5 – Review protocol changes with your doctor before committing to the next cycle
A modified protocol based on failure analysis should be documented and explained before you consent to the next cycle. If your doctor recommends the same protocol without changes: ask specifically what is being changed and why. If no changes are proposed for an identical failure pattern, seek a second opinion.
Learn more : how to make IVF successful first time
Step 6 – Consider a second opinion if you have had 2 or more failures
Two or more IVF failures with good-quality embryos always warrants a fresh perspective. Not because your original clinic is necessarily wrong — but because a second experienced specialist may identify something missed, suggest an investigation not yet done, or recommend a protocol approach your current clinic does not offer.
Book a second opinion at Janisthaa IVF Bangalore
Bring your complete cycle records. Dr. Shwetha will review everything at your first appointment — at no additional records review charge
Second Opinion at Janisthaa IVF: What to Expect
Who should consider a second opinion?
- You have had 2 or more IVF cycles without a successful pregnancy
- Your IVF produced no blastocysts despite good stimulation
- You have been told “nothing more can be done” without advanced investigations
- You have been recommended donor eggs without having had ERA, PGT-A, or endometrial TB screening
- Your previous clinic was in Mysore, Tumkur, Hassan, Kolar, Bellary, Hosur, or another city and you want Bangalore-level specialist care
What Dr. Shwetha reviews at your second opinion consultation
IVF treatment at Janisthaa, the second opinion consultation with Dr. Shwetha Y Baratikka is a 60-minute structured review that covers:
- Complete cycle record analysis – every monitoring data point, embryology record, and transfer note reviewed
- Failure point identification – exactly where in the process the cycle failed
- Gap analysis – which investigations have NOT yet been done that are indicated for your failure pattern
- Protocol redesign – specific changes recommended for the next cycle
- Realistic success rate estimate – based on your profile, after protocol changes
- Cost and timeline – transparent estimate of what the next cycle involves
You leave with a written protocol recommendation that you can implement at Janisthaa IVF or take back to your existing clinic.
For patients travelling from outside Bangalore
Patients from Mysore, Tumkur, Hassan, Mandya, Kolar, Raichur, Bellary, and Hosur frequently come to Janisthaa IVF for second opinion consultations after failed cycles at local clinics. Your first consultation can be conducted by video call using your scanned records. Investigations and any subsequent cycle are then planned around minimising travel most patients come to Bangalore for 3–5 key days per cycle.
The Emotional Reality of IVF Failure - What Couples Experience and What Helps
A failed IVF cycle triggers a grief response that is clinically comparable to pregnancy loss. This is not an overstatement. Research in reproductive psychology documents that couples who experience IVF failure show anxiety and depression levels similar to patients with serious medical diagnoses.
What this means practically:
Allow yourself to grieve. The grief after a failed IVF cycle is real and legitimate. It does not need to be “put in perspective” or minimised. Give yourself and your partner space to feel it — without pressure to “stay positive” or “think about the next cycle.”
Know that grief does not mean loss of hope. The emotional devastation of a failed first or second cycle does not predict the outcome of subsequent cycles. Most couples who persevere through appropriate investigation and protocol changes go on to have successful pregnancies.
Communicate as a couple. IVF failure affects partners differently. Some partners withdraw to protect their partner from their own distress. Some become impatient to “just try again.” Open, non-pressured communication about where each partner is emotionally is more important than any supplement or protocol.
Consider professional support. At Janisthaa IVF, we can refer patients to fertility-specialist counsellors for individual or couple support during and between cycles. This is not a sign of weakness — it is one of the most evidence-supported things a couple can do for their long-term wellbeing during IVF.
Do not make major treatment decisions in the first 2 weeks after a failed cycle. Decisions made in acute grief — switching clinics immediately, abandoning IVF entirely, committing to donor eggs — are often regretted. Allow time for the initial emotional shock to pass before major decisions.
Dr. Shwetha's Clinical Note on IVF Failure
“The conversation I have most often with new patients at Janisthaa IVF is not about their diagnosis — it is about their previous failed cycle. Most of the time, when I review the complete records, I can identify at least one factor that was not investigated or one protocol element that can be meaningfully changed.
The most common things I find in failed cycle records: no endometrial TB screen in a patient from Karnataka or Andhra Pradesh; no ERA testing after two consecutive implantation failures with good embryos; no sperm DNA fragmentation testing despite two cycles of poor embryo quality; and stimulation protocols that were not adjusted after the first failed response.
I do not tell patients this to criticise their previous clinic. I tell them because it means there is almost always something specific to do differently. A failed IVF cycle is devastating. But it is also the most informative thing that has happened in the journey — and at Janisthaa IVF, we use that information.”
— Dr. Shwetha Y Baratikka, Fertility Specialist & IVF Consultant, Janisthaa IVF Bangalore
Book Your Second Opinion or Next Cycle Consultation
If you have experienced an IVF failure — whether your first cycle or your fourth — the next step is a consultation with a specialist who will review your records, identify what went wrong, and design a specific plan for what comes next.
At Janisthaa IVF Bangalore, Dr. Shwetha Y Baratikka brings together over 20 years of fertility specialist experience and an advanced investigation capability — including ERA, PGT-A, endometrial TB screening, NK cell testing, sperm DNA fragmentation, and PRP/G-CSF intrauterine infusion — that many clinics outside Bangalore do not offer.
What you get at your consultation:
- ✅ Complete review of your previous cycle records
- ✅ Identification of the specific failure point and likely cause
- ✅ Customised advanced investigation plan (only what you actually need)
- ✅ Modified protocol designed specifically for your profile
- ✅ Honest success rate estimate after protocol changes
- ✅ Full cost and timeline transparency
Three locations across Bangalore:
- Basaveshwaranagar: 2, 1st Main Rd, 2nd Block
- RR Nagar: 1601, 1st Main Road, BEML Layout
- Nagarbhavi : 525, Second Floor, GM Building, Naagarabaavi 14th Block, 14th Block, NGEF Layout, Nagarbhavi, Bengaluru, Karnataka 560072