Non Invasive Diagnostic of Endometrial Receptivity

Igenomix40 enrolled

Overview

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

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

DIAGNOSTIC

Masking

NONE

Enrollment

Conditions

Endometrial Receptivity Failure

Interventions

Lipid identificationOTHER

The lipids are identified using Mass Spectrometry

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 35 YearsHealthy volunteers:

Medical Language ↔ Plain English

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.

Locations (1)

IVI Valencia

Valencia, Spain

Outcomes

Primary Outcomes

Levels of lipids in the endometrial fluid as a diagnostic factor.

Time frame: 1 year

Data from ClinicalTrials.gov

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