Clinical Trials Directory

Trials / Unknown

UnknownNCT05484193

GnRH Agonist for Luteal Phase Support.

Comparison of Pregnancy Rates After Luteal Phase Support With GnRH Agonist Versus Progesterone - a Prospective Randomized Study

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
150 (actual)
Sponsor
Shaare Zedek Medical Center · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

Objective To assess the the efficacy of luteal support with GnRH agonist in patients undergoing IVF in antagonist-based hcg triggered cycles compared with standard luteal support with progesterone. Design prospective randomized controled study Subjects Patients who underwent antagonist-based cycles performed in the "Shaare Zedek Medical Center" IVF clinic between 2020 and 2022 Intervention Intranasal GnRH-agonist or vaginal Progesterone for luteal support. Main outcome measures Pregnancy and clinical pregnancy rates, ohss. The study cohort included 150 patients who underwent 164 cycles. A total of 127 cycles were included. Of them, 64 were treated with GnRH-a and 63 with progesterone. Hypothesis: This RCT suggests that GnRH-a for luteal phase support is associated with a higher positive β-hCG pregnancy rate and clinical pregnancy rate, compared with standard progesterone support in an antagonist-based protocol triggered with hCG, while maintaining a similar safety profile.

Conditions

Interventions

TypeNameDescription
DRUGGnRH agonistGnRH agonist alone for luteal phase support in fresh IVF embryo transfer cycles
DRUGProgesteronevaginal progesterone for luteal phase support

Timeline

Start date
2020-06-08
Primary completion
2022-04-15
Completion
2023-01-01
First posted
2022-08-02
Last updated
2022-08-02

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT05484193. Inclusion in this directory is not an endorsement.