About this trial
This prospective cohort study aims to compare the effectiveness of half-dose (0.125 mg/day) versus conventional-dose (0.25 mg/day) cetrorelix in GnRH antagonist ICSI cycles regarding clinical pregnancy rate in women with BMI ≥25 kg/m².
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
- Age less than 35 years
Normal ovarian responders (AMH ≥1.2 ng/mL and AFC 5-15)
Body mass index (BMI) ≥25 kg/m²
Written informed consent
Disqualifiers
- Age greater than 35 years
Diminished ovarian reserve (AMH <1.2 ng/mL or AFC <5)
Congenital uterine anomalies or significant intrauterine pathology
Contraindications to ovarian stimulation or pregnancy
Trial population
Women aged less than 35 years with BMI ≥25 kg/m² and normal ovarian reserve who received either half-dose or conventional-dose cetrorelix as part of routine care during GnRH antagonist ICSI cycles at Assiut University Hospital.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Clinical Pregnancy Rate
Proportion of women with intrauterine gestational sac with fetal heartbeat by ultrasound at 6 weeks gestation
Secondary outcomes
Ongoing pregnancy rate
Ongoing pregnancy with heartbeat \>12 weeks on ultrasound
Number of retrieved oocytes
Mean number of oocytes retrieved at pickup
Number of mature MII oocytes
Mean number of mature MII oocytes
Fertilization rate
Fertilized oocytes / MII oocytes
Locations
Sponsors and contacts
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