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Clinical Trials in Egypt / NCT07569315
Starting soon Phase 2

Successive Doses of GnRH Agonist Versus Single Dose of GnRH Agonist to Trigger Ovulation in Hyper-responders

NCT07569315 · tracked via the Priya Life Science Egypt tracker
Phase
Phase 2
Started
2026-06-01
Last updated
2026-05-11

Condition(s) studied

Infertility

Investigational drug(s) / intervention(s)

Successive doses GnRH agonistSingle dose GnRH agonist

Successive doses GnRH agonist: GnRH agonist ( Triptorelin ) ( 0.2 mg / S.C ) is administered 36 hours before ovum pickup. Two additional doses of triptorelin ( 0.1 mg / S.C ) are administered subcutaneously 12 and 24 hours after the first dose of GnRH agonist.

Single dose GnRH agonist: GnRH agonist ( Triptorelin ) ( 0.2 mg / S.C ) is administered 36 hours before ovum pickup.

Study summary

The aim of this randomized controlled study is to compare the efficacy of three successive doses of a GnRH agonist ( administered 36 , 24 and 12 hours before oocyte retrieval ) with a single dose of a GnRH agonist ( administered 36 hours before oocyte retrieval ) in triggering ovulation in hyper-responders

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
40 Years
Healthy volunteers
No
Inclusion Criteria: * GnRH antagonist IVF cycle * Hyper-responders to induction of ovulation Exclusion Criteria: * Hypogonadotrophic hypogonadism * Endometriosis * History of recurrent abortion

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Bedaya Hospital Giza Egypt

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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 NCT07569315 on ClinicalTrials.gov ↗ ← All trials in Egypt