Non Invasive Diagnostic of Endometrial Receptivity

Igenomix

Status: Completed

Conditions: Endometrial Receptivity Failure

Treatments: Other: Lipid identification

Study type: Interventional

Funder types: Industry

Identifiers

NCT01588223

1002-C-069-OB

Details and patient eligibility

About

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

Enrollment: 40 patients

Sex: Female

Ages: 18 to 35 years old

Volunteers: Accepts Healthy Volunteers

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.

Trial design

Primary purpose: Diagnostic

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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40 participants in 1 patient group

Lipids

Experimental group

Treatment:

Other: Lipid identification