CTRI/2017/10/010182
Recruiting
Phase 3
Efficacy of Intrauterine administration of seminal fluid or Human Choronic Gonadotrophin immediately after transvaginal oocyte retrieval on Implantation and pregnancy rate in IVF/ICSI treatment cycles - A randomised double blind trial
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- Infertility patients
- Sponsor
- Bangalore Baptist Hospital
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •The patients undergoing IVF/ICSI treatment at Bangalore Baptist Hospital, Department of Reproductive Medicine Unit as in patients.
- •Inclusion Criteria:
- •1\.Couples undergoing IVF/ICSI cycles with antagonist protocol.
- •2\.Couples undergoing IVF/ICSI cycles with use of partnerâ??s (husband) fresh semen.
- •3\.Couples undergoing IVF/ICSI cycles with female age Ë?38 years.
- •4\.Couples undergoing IVF/ICSI cycles with various semen parameters.
- •5\.Couples undergoing Day 3 Embryo Transfer.
Exclusion Criteria
- •1\.Couples undergoing IVF/ICSI cycles with female age Ë? 38 years.
- •2\.Couples undergoing IVF/ICSI cycles with agonist protocol.
- •3\.Couples undergoing Frozen embryo transfer.
- •4\.Frozen semen samples.
- •5\.Husband undergoing PESA/TESA (Percutaneous Epididymal Sperm Aspiration/Testicular Sperm Aspiration)
- •6\.Poor Ovarian Reserve. AMH(Anti Mullerian Hormone) \<1
- •7\.Couples undergoing Day 5 Embryo Transfer.
Outcomes
Primary Outcomes
Not specified
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