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Trials / Completed

CompletedNCT04724343

Effect of GnRH Agonist vs GnRH Antagonist on IVF/ICSI Outcomes.

Effect of GnRH Agonist (Long Protocol) vs GnRH Antagonist (Flexible Protocol) on IVF/ICSI Outcomes.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Damascus University · Academic / Other
Sex
Female
Age
18 Years – 39 Years
Healthy volunteers
Not accepted

Summary

The aim of this prospective, non-randomised, open-label, clinical trial is to compare the effects of two pituitary suppression regimens; GnRH Agonist-Long Protocol and GnRH Antagonist-Flexible Protocol on clinical and embryological IVF/ICSI outcomes, and on the follicular fluid levels of Placental Growth Factor (PlGF); which is known for his pivotal role in the regulation of ovulation, embryo development, and implantation.

Conditions

Interventions

TypeNameDescription
DRUGTriptorelin acetate0.05-0.1 mg subcutaneously (SC) once daily from the mid-luteal phase (day 21) of the cycle until the day of ovulation triggering.
DRUGCetrorelix0.25 mg subcutaneously (SC) once daily starting from the day detecting a leading follicle diameter ≥ 14 mm until the day of ovulation triggering.
DRUGrecombinant-FSH or recombinant-FSH + human Menopausal GonadotropinDosage adjustment according to the ovarian response.
DRUGHuman Chorionic Gonadotropin (hCG)Ovulation will be triggered by the administration of 10,000 IU of Human Chorionic Gonadotropin (hCG) when at least three follicles become more than 16-17 mm.

Timeline

Start date
2019-12-22
Primary completion
2022-01-01
Completion
2022-07-05
First posted
2021-01-26
Last updated
2023-10-24

Locations

1 site across 1 country: Syria

Source: ClinicalTrials.gov record NCT04724343. Inclusion in this directory is not an endorsement.