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Non Invasive Diagnostic of Endometrial Receptivity

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01588223
First Posted: April 30, 2012
Last Update Posted: March 27, 2014
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 (Responsible Party):
Carlos Simon, Instituto Valenciano de Infertilidad, Spain
  Purpose
The purpose of this study is to determine a lipidomic profile on the endometrial fluid, that can predict endometrial receptivity.

Condition Intervention
Endometrial Receptivity Failure Other: Lipid identification

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: A Non Invasive Diagnostic of Endometrial Receptivity Based on Lipidomic Profile on Endometrial Fluid.

Further study details as provided by Carlos Simon, Instituto Valenciano de Infertilidad, Spain:

Primary Outcome Measures:
  • Levels of lipids in the endometrial fluid as a diagnostic factor. [ Time Frame: 1 year ]

Enrollment: 40
Study Start Date: January 2011
Study Completion Date: May 2012
Primary Completion Date: May 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Lipids Other: Lipid identification
The lipids are identified using Mass Spectrometry

  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 undergoing controlled ovarian stimulation
  • Regular menstrual cycles
  • no abnormal karyotype
  • generally healthy
  • BMI 19-29 Kg/m2 (both inclusive)
  • 18 to 35 years old.

Exclusion criteria:

-patients diagnosed with endometriosis and/or endometritis.

  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): NCT01588223


Locations
Spain
IVI Valencia
Valencia, Spain, 46015
Sponsors and Collaborators
Igenomix
  More Information

Responsible Party: Carlos Simon, Prof. Carlos Simon, MD PhD, Instituto Valenciano de Infertilidad, Spain
ClinicalTrials.gov Identifier: NCT01588223     History of Changes
Other Study ID Numbers: 1002-C-069-OB
First Submitted: April 26, 2012
First Posted: April 30, 2012
Last Update Posted: March 27, 2014
Last Verified: March 2014