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


N/A
18 Years
35 Years
Not Enrolling
Female
Endometrial Receptivity Failure

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Trial Information

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


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.

Type of Study:

Interventional

Study Design:

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Outcome Measure:

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

Outcome Time Frame:

1 year

Safety Issue:

No

Authority:

Spain: Ministry of Health

Study ID:

1002-C-069-OB

NCT ID:

NCT01588223

Start Date:

January 2011

Completion Date:

May 2012

Related Keywords:

  • Endometrial Receptivity Failure
  • Adenoma

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