Successive Doses of GnRH Agonist Versus Single Dose of GnRH Agonist to Trigger Ovulation in Hyper-responders
Starting soon · Phase 2
Conditions studied: Infertility
In brief
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
Key facts
- Study ID
- NCT07569315
- Run by
- Bedaya Hospital
- People needed
- 190
- Starts
- 2026-06-01
- Expected to finish
- 2028-04-01
- Last updated by the study team
- 2026-05-11
Who can join
Age: 18 and older, up to 40. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- GnRH antagonist IVF cycle
- Hyper-responders to induction of ovulation
You may not qualify if…
- Hypogonadotrophic hypogonadism
- Endometriosis
- History of recurrent abortion
Where it is running
- Bedaya Hospital — Giza, Egypt
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.