Trials / Completed
CompletedNCT00830492
Clomiphene Citrate (CC)/Gonadotropin/Gonadotropin Releasing Hormone (GnRH) Antagonist Versus Gonadotropin/GnRH Agonist
Comparisin CC/Gonadotropin/GnRH Antagonist and Gonadotropin/GnRH Agonist in IVF Outcome.
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 200 (estimated)
- Sponsor
- Yazd Research & Clinical Center for Infertility · Academic / Other
- Sex
- Female
- Age
- 18 Years – 35 Years
- Healthy volunteers
- Accepted
Summary
Objective: To compare the efficacy of using mild ovarian stimulation protocol and conventional stimulation protocol in IVF outcome. Design: Prospective randomized trial Setting: University IVF setting. Patient(s): The study compromised a total 200 subinfertile couple that women had regulary menstruation. Intervention(s): Patients were randomized to treatment clomiphene citrate, gonadotropin and GnRH antagonist (100 patients) or GnRH agonist and gonadotropin ( 100 patients). Main outcome measure: Clinical pregnancy rate. Key Words: clomiphene citrate, GnRH agonist, GnRH antagonist, in vitro fertilization, pregnancy rate.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | clomiphene citrate | 100 mg from cycle day 3 through 7 |
| PROCEDURE | Ultrasound | cycle day 8 |
| DRUG | GnRH antagonist | Daily, started with dominant follicle greater than 14 mm (Ganirelix , Organon, Netherlands). |
| DRUG | gonadotopin (HMG) | 75 IU human menopausal gonadotropin (Menogon, ferring, pharmacenticals , Germany) |
| DRUG | buserelin | Buserelin (suprefact, Aventis, Frankfurt, Germany) 500µg subcutaneously (S.C.) everyday for menstrual cycle 21, until the baseline evaluation, which takes place in the first few days of menstruation. If baseline levels of estradiol (\<50 pg/ml ) had been achieved, then the dose of buserelin would be reduced to 250µg. |
| DRUG | rFSH | 150-225 IU recombinant FSH (r\_FSH) (Gonal F, Serono, Aubnne, Switzerland) S.C. |
Timeline
- Start date
- 2008-01-01
- Primary completion
- 2008-12-01
- Completion
- 2008-12-01
- First posted
- 2009-01-28
- Last updated
- 2009-01-28
Locations
1 site across 1 country: Iran
Source: ClinicalTrials.gov record NCT00830492. Inclusion in this directory is not an endorsement.