Non Invasive Diagnostic of Endometrial Receptivity

A Non Invasive Diagnostic of Endometrial Receptivity Based on Lipidomic Profile on Endometrial Fluid.

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01588223

Enrollment

Registered

2012-04-30

Start date

2011-01-31

Completion date

2012-05-31

Last updated

2014-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometrial Receptivity Failure

Brief summary

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

Interventions

OTHERLipid identification

The lipids are identified using Mass Spectrometry

Study design

Allocation

NON_RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

DIAGNOSTIC

Masking

NONE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 35 Years

Healthy volunteers

Yes

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.

Design outcomes

Primary

Measure	Time frame
Levels of lipids in the endometrial fluid as a diagnostic factor.	1 year

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026