This clinical validation study is being carried out to validate the efficacy of a test measuring the clinical application of prostaglandins present in the endometrial fluid in patients, 24 hours before the embryonic transfer. This test is capable of predicting endometrial receptivity without the need of performing a biopsy.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
120
Extraction of endometrial fluid, analysis of prostaglandine and Day 3 embryo transfer
Extraction of endometrial fluid, analysis of prostaglandine and Day 5 embryo transfer
Fundación IVI
Valencia, Valencia, Spain
RECRUITINGIVI Valencia
Valencia, Valencia, Spain
RECRUITINGendometrial receptivity
The endometrial samples will be extracted 24 hours before the embryo transfer in order to analyze the quantity of prostaglandins.
Time frame: 24 hours before embryo transfer
Implantation rate
We will reffer a correlation between the prostaglandin results and the implantation rate.
Time frame: 15 days
Pregnancy rate
We will reffer a correlation between the prostaglandin results and the implantation rate.
Time frame: 15 days
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