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
| Type | Name | Description |
|---|---|---|
| DRUG | Triptorelin acetate | 0.05-0.1 mg subcutaneously (SC) once daily from the mid-luteal phase (day 21) of the cycle until the day of ovulation triggering. |
| DRUG | Cetrorelix | 0.25 mg subcutaneously (SC) once daily starting from the day detecting a leading follicle diameter ≥ 14 mm until the day of ovulation triggering. |
| DRUG | recombinant-FSH or recombinant-FSH + human Menopausal Gonadotropin | Dosage adjustment according to the ovarian response. |
| DRUG | Human 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.