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Clinical Trials in Egypt / NCT07569289
Starting soon Phase 2

Triggering Oocyte Maturation in POSEIDON Group 3 and 4 Poor Responders Using Double Trigger or HCG Trigger

NCT07569289 · tracked via the Priya Life Science Egypt tracker
Phase
Phase 2
Started
2026-06-01
Last updated
2026-05-06

Condition(s) studied

Infertility

Investigational drug(s) / intervention(s)

Double triggerHCG trigger

Double trigger: Triptorelin (0.2 mg/S.C ) and HCG (10000 IU/I.M) are administered 38 to 39 h and 35 to 36 h prior to ovum pick-up., respectively.

HCG trigger: HCG (10000 IU/I.M) is administered 35 to 36 h prior to ovum pick-up.

Study summary

The aim of this randomized controlled study is to compare the efficacy of double trigger protocol \[ the co-administration of GnRH agonist with HCG ( 38 - 39 and 35 - 36 h prior to ovum pick-up, respectively \] with HCG in triggering ovulation in patients with expected poor response to ovarian stimulation

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
40 Years
Healthy volunteers
No
Inclusion Criteria: * POSEIDON group 3 and 4 * GnRH antagonist IVF cycle Exclusion Criteria: * Hypogonadotrophic hypogonadism * Endometriosis * History of recurrent abortion

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Bedaya Hospital Giza Giza Governorate

More Bedaya Hospital trials in Egypt

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 NCT07569289 on ClinicalTrials.gov ↗ ← All trials in Egypt