Clinical Trials Directory

Trials / Completed

CompletedNCT01419353

Programming by Estrogen Treatment in Gonadotropin Releasing Hormone Antagonist Protocol

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
63 (actual)
Sponsor
Meir Medical Center · Academic / Other
Sex
Female
Age
38 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine if pretreatment with Estrogen can assist in the planning and programming of In Vitro Fertilization treatments.

Detailed description

A randomised controlled trial in which study group will be given estrogen derivative before ovarian stimulation in GnRH antagonist protocol and compared to the classical GnRH agonist protocol.Estrogen will be given P.O , "PROGYNOVA' , in a dose of 2 mg /d, starting day 2 of menses and until first Monday to follow. Main outcome measure will be ability to control the ovum pickup day, calculated as a rate of ideal pickups divided by the entire pickup number. All women enrolled will be under 38 years of age, with a clear indication for IVF other than ovulatory dysfunction. women with past 4 treatment failures will be excluded as well as cases in which sperm achieved in surgical methods.

Conditions

Interventions

TypeNameDescription
DRUGestradiol valerate2 mg P.O / day for 1-6 days.

Timeline

Start date
2011-08-01
Primary completion
2013-06-01
Completion
2013-06-01
First posted
2011-08-18
Last updated
2013-12-24

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01419353. Inclusion in this directory is not an endorsement.

Programming by Estrogen Treatment in Gonadotropin Releasing Hormone Antagonist Protocol (NCT01419353) · Clinical Trials Directory