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Clinical Trials/NCT01385332
NCT01385332
Completed
Not Applicable

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

Parc de Salut Mar1 site in 1 country10 target enrollmentMarch 2010
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ConditionsStimulation in the Ovary

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stimulation in the Ovary
Sponsor
Parc de Salut Mar
Enrollment
10
Locations
1
Primary Endpoint
Number of eggs
Status
Completed
Last Updated
8 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

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.

Registry
clinicaltrials.gov
Start Date
March 2010
End Date
September 2012
Last Updated
8 years ago
Study Type
Interventional
Study Design
Crossover
Sex
Female

Investigators

Sponsor
Parc de Salut Mar
Responsible Party
Principal Investigator
Principal Investigator

Miguel Angel Checa

MD

Parc de Salut Mar

Eligibility Criteria

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

Outcomes

Primary Outcomes

Number of eggs

Time Frame: 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.

Study Sites (1)

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