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GnRH for Luteal Support in IVF/ICSI/FET Cycles

GnRH for Luteal Support in IVF/ICSI/FET Cycles

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02357654
Enrollment
350
Registered
2015-02-06
Start date
2015-11-30
Completion date
2026-07-31
Last updated
2025-08-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility

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 .

Detailed description

see above

Interventions

DRUGGnRH

single shot of GnRH agonist

DRUGplacebo

placebo

Sponsors

University Reproductive Associates
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* day 3 transfers

Design outcomes

Primary

MeasureTime frame
Live birth per transfer9 months

Secondary

MeasureTime frame
implantation rates4 weeks
clinical pregnancy4 weeks
rates of OHSS4 weeks

Countries

United States

Contacts

Primary ContactPeter G McGovern, MD
mcgovepg@gmail.com201-288-6330

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026