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Effect of Premature Luteinization on the Oocyte Quality in Oocyte Donation Program.

This study has been completed.

Sponsored by: Instituto Valenciano de Infertilidad, Spain
Information provided by: Instituto Valenciano de Infertilidad, Spain
ClinicalTrials.gov Identifier: NCT00455949
  Purpose

Analyze the possible effect of the progesterone levels of the hCG administration on the oocyte embryo quality. The primary endpoint of this study is the pregnancy rate.


Condition
Premature Luteinization

U.S. FDA Resources

Study Type:   Observational
Study Design:   Longitudinal, Defined Population, Prospective Study
  Eligibility
Ages Eligible for Study:   18 Years to 34 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria:

  • Oocyte donors; age range: 18 - 34; BMI: 18 - 29; long protocol.

Exclusion Criteria:

  • PCO syndrome;
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00455949

Locations
Spain
Instituto Valenciano de la Infertilidad    
      Valencia, Spain, 46015

Sponsors and Collaborators
Instituto Valenciano de Infertilidad, Spain

Investigators
Principal Investigator:     Marco Melo, MD     Instituto Valenciano de Infertilidad    
Principal Investigator:     Marco Melo, MD     Instituto Valenciano de Infertilidad    
  More Information


Study ID Numbers:   VLC-MM-0106-307-14
First Received:   April 3, 2007
Last Updated:   April 3, 2007
ClinicalTrials.gov Identifier:   NCT00455949
Health Authority:   Spain: Ministry of Health

ClinicalTrials.gov processed this record on October 22, 2008




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