Non Invasive Diagnostic of Endometrial Receptivity

NCT01588223 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2014-03-27

No results posted yet for this study

Summary

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

Conditions

  • Endometrial Receptivity Failure

Interventions

OTHER

Lipid identification

The lipids are identified using Mass Spectrometry

Sponsors & Collaborators

  • Igenomix

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-01-31
Primary Completion
2012-05-31
Completion
2012-05-31

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01588223 on ClinicalTrials.gov