A Comparative Study of Two Patterns of Controlled Ovarian Hyperstimulation in Mid Follicular Phase or Early Luteal Phase for Egg Donors
Not Applicable
Completed
- Conditions
- Stimulation in the Ovary
- Interventions
- Procedure: Early luteal phaseProcedure: Late follicular phase -COH-
- Registration Number
- NCT01385332
- Lead Sponsor
- Parc de Salut Mar
- Brief 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 10
Inclusion Criteria
- premenopausal women 18-30 years old, with FSH levels < 10mIU
- irregular menstrual cycle
- BMI between 12-28
- signed inform consent
Exclusion Criteria
- Polycystic ovarian syndrome, gonadotropins allergy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Early luteal phase -COH- Early luteal phase We perform an standard antagonist protocol beginning the second day of the menstrual cycle compared with an antagonist protocol beginning in the early luteal phase. Late folicular phase - COH - Late follicular phase -COH- We perform an standard antagonist protocol beginning the second day of the menstrual cycle compared with an antagonist protocol beginning in the late follicular phase.
- Primary Outcome Measures
Name Time Method Number of eggs Participants will be followed after 1-3 hrs of follicular aspiration. The results will be presented in one year, egg recipients will be followed until 12 weeks of pregnancy.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Servei de Ginecologia i Obstetricia, Hospital del Mar-Parc Salut Mar
🇪🇸Barcelona, Spain