Recruiting

Progesterone with GnRH Agonist

Sponsor:

University Reproductive Associates

Code:

NCT02357654

Conditions

Infertility

Eligibility Criteria

Sex: Female

Age: 18 - 40

Healthy Volunteers: Not accepted

Interventions

GnRH

placebo

Study Details

Brief summary:

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 .

Conditions

Infertility

Study ID

NCT02357654

Start date

Nov, 2015

Status verified date

Jul, 2026

Completion date

Jul, 2026

Anticipated

Primary completion date

Jul, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Female

Age: 18 - 40

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • women undergoing IVF/ICSI or frozen embryo transfers (FET) that less than 40 years old.

Exclusion Criteria:

  • day 3 transfers

Study Design

Enrollment

350 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: GnRH agonist

placebo comparator: Placebo

Interventions

GnRH

single shot of GnRH agonist

placebo

placebo

Primary outcome measure

  • Live birth per transfer [ Time Frame: 9 months ]

Central Contacts and Locations

Central contacts

Locations

University Reproductive Associates

Recruiting

Hasbrouck Heights, New Jersey, United States, 07604

Principal Investigator:

Peter G. McGovern, MD

More Information

Sponsor

University Reproductive Associates

Last update posted

Jul 9, 2026

Last verified

Jul, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-03. This information was provided to ClinicalTrials.gov by University Reproductive Associates on 2026-07-09.