Impact of chronic endometritis in endometrial receptivity and the prediction of the personalized window of implantation: a prospective before-and-after study

Not Applicable

Recruiting

• Conditions: Infertility

• Registration Number: JPRN-UMIN000046909
• Lead Sponsor: Igenomix Foundation

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-02-15
• Study Completion: 2023-05-31
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 240

Inclusion Criteria

Not provided

Exclusion Criteria

Patients who are IUD carriers in the 3 months prior to the first biopsy for EMMA test. Patients who have taken prescribed antibiotics in the last 3 months prior to the first biopsy for EMMA test. Cases where the patient has received previous prophylactic antibiotics (1 single dose) to ovarian puncture in the stimulation cycle may be accepted. The administration of this prophylactic antibiotic should be at least 1 month before the sample collection (first biopsy for the EMMA test). Patients that received any surgical procedure in the 3 months prior to the first biopsy for EMMA test. Patients that present a different endometrial preparation (HRT) for the different cycles included in the study (1st mock cycle, 2nd mock cycle, ET cycle) in terms of P4 dosage, timing or route of administration. Patients with endogenous P4 >1ng/mL determined at day P+0 of the HRT cycles included in the study (1st mock cycle, 2nd mock cycle, ET cycle) or with unknow levels of endogenous P4 before the administration exogenous progesterone in any of the HRT cycles included in the study. Patients receiving personalized ET with embryos other than blastocyst in days 5 or 6. Patients cured of CE that do not follow the recommendations of the 2nd ERA test for pET. And others.

Study & Design

• Study Type: Observational
• Study Design: Not specified