Bedaya Hospital
Giza, Giza Governorate, 3753303, Egypt
Location contact
Reham Elkhalifa, M.D, PhD
PRINCIPAL_INVESTIGATOR
Usama M Fouda, Prof
CONTACT
NCT Number: NCT07569289
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
Trial opening soon.
Get Notified18 year–40 year
Female
Interventional
Phase 2
Giza, Giza Governorate, 3753303, Egypt
Reham Elkhalifa, 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
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 (10000 IU/I.M) is administered 35 to 36 h prior to ovum pick-up.
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 Oocyte Maturation in POSEIDON Group 3 and 4 Poor Responders Using Double Trigger or HCG Trigger . A Randomized Controlled Study
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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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