Non Invasive Diagnostic of Endometrial Receptivity

Not Applicable

Completed

• Conditions: Endometrial Receptivity Failure
• Interventions: Other: Lipid identification

• Registration Number: NCT01588223
• Lead Sponsor: Igenomix

Brief Summary

The purpose of this study is to determine a lipidomic profile on the endometrial fluid, that can predict endometrial receptivity.

Detailed Description

Not available

Study Timeline

• Study Start: 2011-01
• Study First Submitted: 2012-04-26
• Study First Submitted QC: 2012-04-27
• Study First Posted: 2012-04-30
• Primary Completion: 2012-05
• Study Completion: 2012-05
• Status Verified: 2014-03
• Last Update Submitted: 2014-03-26
• Last Update Posted: 2014-03-27

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 40

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.

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Lipids	Lipid identification	-

Primary Outcome Measures

Name	Time	Method
Levels of lipids in the endometrial fluid as a diagnostic factor.	1 year

Trial Locations

Locations (1)

IVI Valencia; 🇪🇸 Valencia, Spain