Endometrial Gene Expression Profile in Controlled Ovarian Stimulation Cycles With Premature Luteinization
Primary Purpose
Premature Luteinization
Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
endometrial biopsy
Sponsored by

About this trial
This is an interventional trial for Premature Luteinization
Eligibility 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
Sites / Locations
- Ivi Valencia
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00447850
First Posted
March 13, 2007
Last Updated
September 18, 2009
Sponsor
Instituto Valenciano de Infertilidad, IVI VALENCIA
1. Study Identification
Unique Protocol Identification Number
NCT00447850
Brief Title
Endometrial Gene Expression Profile in Controlled Ovarian Stimulation Cycles With Premature Luteinization
Official Title
Endometrial Gene Expression Profile in Controlled Ovarian Stimulation Cycles With Premature Luteinization
Study Type
Interventional
2. Study Status
Record Verification Date
September 2009
Overall Recruitment Status
Completed
Study Start Date
April 2007 (undefined)
Primary Completion Date
July 2009 (Actual)
Study Completion Date
July 2009 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Instituto Valenciano de Infertilidad, IVI VALENCIA
4. Oversight
5. Study Description
Brief Summary
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Premature Luteinization
7. Study Design
Study Phase
Not Applicable
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
endometrial biopsy
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elena Labarta, MD
Organizational Affiliation
Instituto Valenciano de la Infertilidad
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ivi Valencia
City
Valencia
ZIP/Postal Code
46015
Country
Spain
12. IPD Sharing Statement
Learn more about this trial
Endometrial Gene Expression Profile in Controlled Ovarian Stimulation Cycles With Premature Luteinization
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