Clinical Trials Directory

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

TypeNameDescription
DRUGclomiphene citrate100 mg from cycle day 3 through 7
PROCEDUREUltrasoundcycle day 8
DRUGGnRH antagonistDaily, started with dominant follicle greater than 14 mm (Ganirelix , Organon, Netherlands).
DRUGgonadotopin (HMG)75 IU human menopausal gonadotropin (Menogon, ferring, pharmacenticals , Germany)
DRUGbuserelinBuserelin (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.
DRUGrFSH150-225 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.