Evaluation of the effect of oral levofloxacin on chronic endometritis in patients

Phase 3

• Conditions: Endometritis.; Inflammatory disease of uterus, unspecified; N71.9

• Registration Number: IRCT20220413054524N1
• 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: 30 May 2022

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

Females with chronic endometritis with fetal transfer failure confirmed by histology using histology

Exclusion Criteria

Sensitivity to doxycycline
Allergy to metronidazole
Glucose 6 phosphate dehydrogenase deficiency

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Endometritis. Timepoint: Before the intervention and the next menstrual cycle. Method of measurement: Perform a biopsy.