DRUG
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.
Status
Not yet recruiting
Phase
Phase 2
Enrollment
164
Locations
1
Results
Not posted
Publications
0
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
Interventions
DRUG
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.
DRUG
HCG (10000 IU/I.M) is administered 35 to 36 h prior to ovum pick-up.
Timeline
First posted
May 6, 2026
Study start
Jun 1, 2026
Primary completion
Dec 1, 2027
Study completion
Apr 1, 2028
Results posted
Not reported
Registry updated
May 6, 2026
Outcomes
Metaphase-II oocytes rate
Time frame · Ten to fifteen days after starting ovarian stimulation
Number of MII oocyte/ number of cumulus oocyte complex
Clinical pregnancy rate
Time frame · Five weeks after embryo transfer
Presence of intrauterine gestational sac detected by transvaginal ultrasound
Ongoing pregnancy Rate
Time frame · Eighteen weeks after embryo transfer
Pregnancies continued beyond 20 weeks gestation
Eligibility
Inclusion Criteria: * POSEIDON group 3 and 4 * GnRH antagonist IVF cycle Exclusion Criteria: * Hypogonadotrophic hypogonadism * Endometriosis * History of recurrent abortion
Study locations
Egypt. Showing up to 24 locations stored in the fast local snapshot.
Bedaya Hospital
Giza, Giza Governorate, Egypt
Publications
No PMID-linked publications were present in this registry snapshot.
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