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Effect of Topical Metronidazole in treatment of chronic fissure

Phase 3
Recruiting
Conditions
Chronic Anal Fissure.
Chronic anal fissure
K60.1
Registration Number
IRCT20221102056377N1
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
54
Inclusion Criteria

All individuals with anal fissures for more than 6 weeks

Exclusion Criteria

Suffering from other colorectal diseases
The person is unable to participate in follow-up visits
Duration of symptoms less than 6 weeks

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Determination of pain intensity in patients with chronic anal fissure treated with Metronidazole gel and diltiazem. Timepoint: Determination of pain intensity in patients with chronic anal fissure at the beginning of the study and 10, 21, 28 days after starting Metronidazole. Method of measurement: Examination of Anus; Use of Visual Analogue Scale.;Determining the duration of pain in patients with chronic anal fissure treated with Metronidazole gel and Diltiazem. Timepoint: Determining the duration of pain in patients with chronic anal fissure at the beginning of the study and 10, 21, 28 days after starting Metronidazole. Method of measurement: Questionnaire.
Secondary Outcome Measures
NameTimeMethod
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