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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Early luteal phase | We 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. |
| PROCEDURE | Late 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.