Clinical Trials Directory

Trials / Completed

CompletedNCT01385332

A Comparative Study of Two Patterns of Controlled Ovarian Hyperstimulation in Mid Follicular Phase or Early Luteal Phase for Egg Donors

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Parc de Salut Mar · Academic / Other
Sex
Female
Age
18 Years – 30 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine the efficacy and safety of two new patterns of controlled ovarian hyperstimulation (defined as total number of picked up eggs). This study will be performed in egg donors but these new patterns will be implemented in fertility preservation patients.

Conditions

Interventions

TypeNameDescription
PROCEDUREEarly luteal phaseWe will administer in the tenth day of the cycle 0.25mg/day of ganirelix until the estradiol levels will be less than 60pgr/mL. Then, we'll start a standard protocol of controlled ovarian hyperstimulation beginning with 150 UI/day. At 6th day of stimulation we'll begin with the antagonist.
PROCEDURELate follicular phase -COH-We will administer in the 20th day of the cycle 0.25mg/day of ganirelix until the estradiol levels will be less than 60pgr/mL. Then, we'll start a standard protocol of controlled ovarian hyperstimulation beginning with 150 UI/day. At 6th day of stimulation we'll begin with the antagonist.

Timeline

Start date
2010-03-01
Primary completion
2012-06-01
Completion
2012-09-01
First posted
2011-06-30
Last updated
2017-09-20

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT01385332. Inclusion in this directory is not an endorsement.