Evaluating the Efficacy of Diltiazem Gel in Reducing the Complications and Pain in Anorectal Operations

Phase 3

• Conditions: Anorectal surgery.; Anorectal fistula; K60.5

• Registration Number: IRCT20120118008769N5
• Lead Sponsor: Ghoum University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 11 January 2022

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 144

Inclusion Criteria

Candidates for anorectal surgery
Informed consent

Exclusion Criteria

Pregnant women
Sensitivity to diltiazem gel

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative pain score. Timepoint: Immediately after surgery then every 8 hours to 24 hours. Method of measurement: Visual Analogue Scale.