The effects of ciprofloxacin on the treatment of bacterial otitis media

Phase 3

• Conditions: Chronic bacterial otitis media.; Chronic mucoid otitis media; H65.3

• Registration Number: IRCT20130427013136N7
• Lead Sponsor: Babol University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 March 2020

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

Patients with chronic bacterial otitis media

Exclusion Criteria

Suspected Patients to mixed bacterial and fungal otitis
Suspected Patients to otomycosis
patients with external otitis
patients without rupture of the eardrum

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Before intervention and 2 weeks after intervention. Method of measurement: Severity of pain will determined by the patient's expression or pain index (Visual Analog Scale-VAS) which are between 0-10.;Swelling. Timepoint: Before intervention and 2 weeks after intervention. Method of measurement: Severity of swelling will determine based on the examination of the ear by the physician.;Discharge. Timepoint: Before intervention and 2 weeks after intervention. Method of measurement: Severity of discharge will determine based on the examination of the ear by the physician.