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Clinical Trial of Anusol Ointment for Symptom Relief in Patients With Haemorrhoids

Hemorrhoids Clinical Trial

Official title:
A Randomized, Placebo- and Benchmark-controlled, Double-blind Clinical Trial of Anusol Topical Ointment to Evaluate Symptom Relief in Patients With Haemorrhoids

Clinical Trial Summary

The purpose of this study is to assess the efficacy and safety of Anusol topical ointment for the relief of internal and external haemorrhoid symptoms in people with Grades I-III haemorrhoids compared to a placebo (the study medication without the active ingredients) and a benchmark product.

Clinical Trial Description

Adult patients with haemorrhoids meeting all the eligibility criteria will be allocated in three study arms: test, placebo and benchmark. Approximately twenty-two subjects per group will be enrolled to assure that approximately 20 subjects in each group complete the study. The study will be conducted in Armenia.The study will last approximately 2 weeks for each subject and will consist of 3 visits. The first subject first visit is planned for June 2021, and the study will continue until the target sample size is reached. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05157711
Study type Interventional
Source Church & Dwight Company, Inc.
Contact
Status Completed
Phase Phase 3
Start date November 25, 2021
Completion date March 31, 2022
View Details
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