Metronidazole vaginal gel and surgical site infectio

Phase 2

Recruiting

• Conditions: Infection of obstetric surgical wound; Surgical site infection.; O86.0

• Registration Number: IRCT20200217046523N9
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 100

Inclusion Criteria

Candidate for elective hysterectomy
Obtaining written consent

Exclusion Criteria

Hysterectomy followed by cesarean section
Hysterectomy following a normal delivery
Emergency hysterectomies
Patients who have received broad-spectrum antibiotics before surgery
Patient dissatisfaction
Infection of the patient with vaginitis with cervicitis in the preoperative period

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Infection. Timepoint: Two weeks and six weeks after surgery. Method of measurement: Examination and patient history.