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Clinical Trial Summary

the main aim of this study is to clinically assess the effectiveness of topical chamomile oral gel in the prevention of chemotherapy-induced oral mucositis.


Clinical Trial Description

The study was designed as a randomized, controlled, clinical trial. patients who were undergoing to receive chemotherapy were divided into three groups: Group I: was given conventional treatment. Group II: was given topical oral gel of chamomile. Group III: was given topical oral gel of chamomile in combination with the conventional treatment.

All patients have clinically evaluated at the start of the chemotherapy and three weeks later for pain and oral mucositis severity. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04317183
Study type Interventional
Source Alexandria University
Contact Mahmoud Elhadad, BDS
Phone 01009394469
Email elhadad2008@gmail.com
Status Recruiting
Phase Phase 2
Start date May 15, 2019
Completion date March 30, 2020