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