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NOT YET RECRUITING
NCT06212102
PHASE2

Dydrogesterone Versus GnRH Antagonist in Poor Responders Undergoing Double Ovarian Stimulation

Sponsor: Bedaya Hospital

View on ClinicalTrials.gov

Summary

The aim of this randomized controlled trial was to compare the efficacy and cost-effectiveness of using progestin with GnRH antagonist to prevent premature LH surge in poor responders undergoing double stimulation protocol.

Official title: Dydrogesterone Versus GnRH Antagonist in Poor Responders Undergoing Double Ovarian Stimulation: A Randomized Controlled Non-inferiority Trial

Key Details

Gender

FEMALE

Age Range

35 Years - 44 Years

Study Type

INTERVENTIONAL

Enrollment

120

Start Date

2024-02

Completion Date

2026-12

Last Updated

2024-01-23

Healthy Volunteers

No

Conditions

Interventions

DRUG

Progestin primed ovarian stimulation

HMG ( 300IU) was used during the follicular phase of ovarian stimulation (FPS) and during the luteal phase of ovarian stimulation (LPS). Progestin (dydrogesterone) 30 mg/day was used to prevent premature LH surge during the FPS and LPS.

DRUG

GnRH antagonist

HMG ( 300IU) was used during the follicular phase of ovarian stimulation (FPS) and during the luteal phase of ovarian stimulation (LPS). Flexible GnRH antagonist protocol (Cetrorelix acetate) (0.2 mg) was used to prevent premature LH surge during the FPS and LPS.

Locations (1)

Bedaya Hospital

Giza, Egypt