Clinical Trial

rFSH vs rFSH+rLH in Dydrogesterone-Based Progestin Protocol: A Prospective Study

Study acronym: DYG-GONA
Completed
View on ClinicalTrials.gov →
Summary
This study aims to compare two commonly used hormone treatments for women undergoing IVF. All participants will receive a stimulation protocol that includes dydrogesterone, a medication used to safely control natural hormone surges during treatment. The study will observe women who are treated either with recombinant FSH alone or with a combination of recombinant FSH and recombinant LH-both routinely used options in our clinic. Investigators will prospectively monitor how these treatments affect the growth of ovarian follicles, the number of mature eggs collected, the quality of developing embryos, and early pregnancy outcomes. No additional procedures or medications will be required beyond standard IVF care. The goal is to better understand whether adding recombinant LH provides any measurable benefit in dydrogesterone-based PPOS cycles.
Protocol Amendment History 4 changes
critical Trial completed 2026-06-25
notable Enrollment reduced: 300 -> 202 participants 2026-06-25
notable Primary completion pushed: 2026-04-30 -> 2026-06-15 2026-06-25
minor Completion pushed: 2026-05-10 -> 2026-06-20 2026-06-25
Trial Details
NCT Number NCT07348757
Lead Sponsor Centrum Clinic IVF Center
Conditions InVitro Fertilization, Gonadotropins
Enrollment 202 participants
Start Date 2026-02-05
Primary Completion 2026-06-15 (estimated)
Study Completion 2026-06-20 (estimated)
Updated on ClinicalTrials.gov 2026-06-24