MedPath

To find out whether instillation of seminal fluid or drug (hCG) into the uterus will result in increased pregnancy rates

Phase 3
Conditions
Health Condition 1: null- Infertility patients
Registration Number
CTRI/2017/10/010182
Lead Sponsor
Bangalore Baptist Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
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.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
percentage of implantation rateTimepoint: percentage of implantation rate. <br/ ><br>(within 6 weeks of IVF pregnancy).
Secondary Outcome Measures
NameTimeMethod
percentage of clinical and ongoing pregnancy rateTimepoint: percentage of clinical and ongoing pregnancy rate. (Clinical pregnancy within 18days of Transvaginal oocyte retrieval and ongoing pregnancy rate within 12 weeks of IVF pregnancy.
© Copyright 2025. All Rights Reserved by MedPath