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Clinical Trials in Egypt / NCT06212102
Recruiting Phase 2

Dydrogesterone Versus GnRH Antagonist in Poor Responders Undergoing Double Ovarian Stimulation

NCT06212102 · tracked via the Priya Life Science Egypt tracker
Phase
Phase 2
Started
2024-05-08
Last updated
2026-05-04

Condition(s) studied

Infertility

Investigational drug(s) / intervention(s)

Progestin primed ovarian stimulationGnRH antagonist

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.

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.

Study summary

The aim of this randomized controlled trial is 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.

Eligibility

Sex
FEMALE
Min age
35 Years
Max age
44 Years
Healthy volunteers
No
Inclusion Criteria: Patients belonging to Poseidon group 4 Exclusion Criteria: * PCOS * Endometriosis * History of recurrent abortion

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Cairo University Cairo Cairo Governorate Recruiting
Bedaya Hospital Giza Egypt Not Yet Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06212102 on ClinicalTrials.gov ↗ ← All trials in Egypt