Skip to main content
Clinical Trials/CTRI/2017/10/010182
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

Bangalore Baptist Hospital0 sites0 target enrollmentTBD

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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

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

Similar Trials