Evaluating 5ASA efficacy in treatment of symptomatic hemorrhoid

Phase 2

Recruiting

• Conditions: hemorrhoids.; Unspecified haemorrhoids without complication; I84.9

• Registration Number: IRCT20191226045897N2
• 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: 26 May 2021

Recruitment & Eligibility

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

Inclusion Criteria

Sigmoidoscopy
Hemorrhoids based on clinical indicators and examination

Exclusion Criteria

Hemorrhoids stage 3 and up
Ulcerative proctitis
Pregnancy or breastfeeding
Allergy to salicylates
Liver dysfunction
Renal dysfunction

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Bleeding. Timepoint: Before intervention, 2 weeks after the initial intervention. Method of measurement: questionnaire.;Pain. Timepoint: Before intervention, 2 weeks after the initial intervention. Method of measurement: questionnaire.;Anal burning. Timepoint: Before intervention, 2 weeks after the initial intervention. Method of measurement: questionnaire.