GnRH for Luteal Support in IVF/ICSI/FET Cycles
Part of paid clinical trials in Hasbrouck Heights, New Jersey.
- Sponsor
- University Reproductive Associates
- Study ID
- NCT02357654
- Phase
- PHASE4
- Status
- Recruiting
Conditions
- Infertility
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - 40 Years
- Healthy Volunteers
- Not accepted
Interventions
- GnRH — DRUGsingle shot of GnRH agonist
- placebo — DRUGplacebo
Study Details
During IVF cycles an embryo is generally placed into the uterine cavity between 3 and 5 days after fertilization. For a successful pregnancy to take place, that embryo must then implant in the properly primed and staged endometrium, which subsequently must continue to develop to accommodate the growing and maturing embryo and then fetus. This process is normally regulated by hormonal interactions between the fetal, endometrial and luteal tissue. It has been found that after IVF additional support for the endometrium with progesterone improves implantation and subsequent live birth rates in IVF cycle . Recent data has shown that additional supplementation with a single administration of a GnRH agonist around the time the time of embryo transfer may further enhance these rates .
Key Dates
- Start date
- Nov 30, 2015
- Status verified
- Jul 2025
- Primary completion
- Jul 31, 2026
- Completion
- Jul 31, 2026
Study Design
- Enrollment
- 350 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: GnRH agonist
- Placebo Comparator: Placebo
Primary Outcome Measure
Live birth per transfer [ Time Frame: 9 months ]
Central Contacts
- Peter G McGovern, MD201-288-6330
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University Reproductive Associates | Hasbrouck Heights | New Jersey | 07604 | Peter G. McGovern, MD (PRINCIPAL_INVESTIGATOR) |
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