acyclovir in anal fissure

Phase 3

Recruiting

• Conditions: Anal fissures.; Anal fissure, unspecified; K60.2

• Registration Number: IRCT20200906048636N1
• Lead Sponsor: Tabriz 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: Recruiting
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

Patients' informed consent to participate in the study
No previous or current history of HSV and other STDs
Adults over the age of 18
Referral patients with clinical diagnosis of anal fissure

Exclusion Criteria

Have a previous or current history of HSV and other perinatal STDs
Patient dissatisfaction to participate in the study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain relief assessed based on numerical rating scale (NRS). Timepoint: before intervention and 2, 3 , 4, 8, 12 weeks after intervention. Method of measurement: Checklist based on NRS.