Bedaya Hospital
Giza, Giza Governorate, 3753303, Egypt
Location contact
Amira Alasmar, M.D, PhD
PRINCIPAL_INVESTIGATOR
Usama M Fouda, Prof
CONTACT
NCT Number: NCT07569302
The aim of this randomized controlled study is to compare the efficacy of a modified dual trigger protocol [a single bolos of HCG combined with two successive doses of a GnRH agonist ] with HCG [a single bolos administered 36 hours before oocyte retrieval ] in triggering ovulation in normo-responders undergoing ovarian stimulation using the antagonist protocol.
Trial opening soon.
Get Notified18 year–40 year
Female
Interventional
Phase 2
Giza, Giza Governorate, 3753303, Egypt
Amira Alasmar, M.D, PhD
PRINCIPAL_INVESTIGATOR
Usama M Fouda, Prof
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
HCG (10000 IU /IM) and triptorelin (0.2 mg/S.C) are administered 36 hours before ovum pickup . Moreover, 0.1mg of triptorelin is administered 24 h prior to ovum pick-up.
HCG (10000 IU/IM ) is administered 36 hours before ovum pickup.
Time frame: Ten to fifteen days after starting ovarian stimulation
Number of MII oocyte/ number of cumulus oocyte complex
Time frame: Five weeks after embryo transfer
Presence of intrauterine gestational sac detected by transvaginal ultrasound
Time frame: Eighteen weeks after embryo transfer
Pregnancies continued beyond 20 weeks gestation
Contact information is provided by the study sponsor or research team.
Bedaya Hospital
Other
Triggering Ovulation in Normo-responders Using a Modified Dual Trigger Protocol or HCG Trigger . A Randomized Controlled Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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