Evaluation of the effect of intrauterine injection of ciprofloxacin on chronic endometritis

Phase 3

Recruiting

• Conditions: Endometritis - Recurrent implantation failure.; Endometriosis of uterus; N80.0

• Registration Number: IRCT20230111057108N1
• Lead Sponsor: Shahre-kord University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 13 March 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 30

Inclusion Criteria

Informed consent to participate in the study
Women with chronic endometritis with embryo transfer failure
Confirmation of infection using histology and hysteroscopy
At least 3 with unsuccessful embryo transfer without genetic, metabolic or endocrine causes

Exclusion Criteria

Hypersensitivity to doxycycline and ciprofloxacin
Unwillingness to continue participating in the study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction of histological symptoms related to endometritis. Timepoint: Before and one month after receiving the medicine. Method of measurement: Laboratory (mild-moderate-severe).

Secondary Outcome Measures

Name	Time	Method
Increase the chance of fertility. Timepoint: After receiving the medicine. Method of measurement: Fertility percentage.