- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00447850
Endometrial Gene Expression Profile in Controlled Ovarian Stimulation Cycles With Premature Luteinization
September 18, 2009 updated by: Instituto Valenciano de Infertilidad, IVI VALENCIA
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Valencia, Spain, 46015
- IVI Valencia
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 35 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Elena Labarta, MD, Instituto Valenciano de la Infertilidad
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2007
Primary Completion (ACTUAL)
July 1, 2009
Study Completion (ACTUAL)
July 1, 2009
Study Registration Dates
First Submitted
March 13, 2007
First Submitted That Met QC Criteria
March 13, 2007
First Posted (ESTIMATE)
March 15, 2007
Study Record Updates
Last Update Posted (ESTIMATE)
September 21, 2009
Last Update Submitted That Met QC Criteria
September 18, 2009
Last Verified
September 1, 2009
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- VLC-EL-1006- 307-2
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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University of OklahomaIndiana University School of MedicineCompletedPreterm Premature Rupture of Membranes
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University of CalgaryCanadian Institutes of Health Research (CIHR); Alberta Economic Development...TerminatedMicrobiota | Gastrointestinal Microbiome | Infant, Premature | Infants, Extremely PrematureCanada
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Clinical Trials on endometrial biopsy
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University of Sao PauloConselho Nacional de Desenvolvimento Científico e TecnológicoTerminated
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Clinique OvoActive, not recruiting
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McGill UniversityUnknown
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Duke UniversityUniversity of Illinois at ChicagoCompleted
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Selçuk UniversityCompleted
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Brown FertilityWithdrawnRecurrent Implantation Failure in Setting of Artifically Prepared Endometrium
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Cairo UniversityUnknownRIF , Endometrial Receptivity