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Endometrial Gene Expression Profile in Controlled Ovarian Stimulation Cycles With Premature Luteinization

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00447850
First Posted: March 15, 2007
Last Update Posted: September 21, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Instituto Valenciano de Infertilidad, IVI VALENCIA
  Purpose
Previous studies have suggested that premature luteinization (PL)during controlled ovarian stimulation (COS) decreases the implantation rate due to a negative effect on the endometrium receptivity. This study aims to describe the impact on endometrial gene expression of PL in GnRH antagonist and GnRH agonist cycles.

Condition Intervention
Premature Luteinization Procedure: endometrial biopsy

Study Type: Interventional
Official Title: Endometrial Gene Expression Profile in Controlled Ovarian Stimulation Cycles With Premature Luteinization

Resource links provided by NLM:


Further study details as provided by Instituto Valenciano de Infertilidad, IVI VALENCIA:

Study Start Date: April 2007
Study Completion Date: July 2009
Primary Completion Date: July 2009 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 35 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Oocyte donors
  • Age between 18-35 years old
  • BMI 18-29
  • NORMOGONADOTROPHICS
  • PROGESTERONE ≥ 1.2 ng/ml on hCG day

Exclusion Criteria:

  • PolyCystic Ovarian Syndrome (PCOS)
  • Endometriosis
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00447850


Locations
Spain
Ivi Valencia
Valencia, Spain, 46015
Sponsors and Collaborators
Instituto Valenciano de Infertilidad, IVI VALENCIA
Investigators
Principal Investigator: Elena Labarta, MD Instituto Valenciano de la Infertilidad
  More Information

Responsible Party: Dr. Elena Labarta, Instituto Valenciano de Infertilidad
ClinicalTrials.gov Identifier: NCT00447850     History of Changes
Other Study ID Numbers: VLC-EL-1006- 307-2
First Submitted: March 13, 2007
First Posted: March 15, 2007
Last Update Posted: September 21, 2009
Last Verified: September 2009

Additional relevant MeSH terms:
Premature Birth
Obstetric Labor, Premature
Obstetric Labor Complications
Pregnancy Complications