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The Use of Tulsi Extract for The Management of Oral Mucositis in Head & Neck Cancer Patients Undergoing Radiotherapy

Stomatitis Clinical Trial

Official title:
The Use of Tulsi Extract for The Management of Oral Mucositis in Head & Neck Cancer Patients Undergoing Radiotherapy: A Randomized Clinical Trial

Clinical Trial Summary

After signing the informed consent, the participant will be allocated to either intervention or control group, then each participant will use either 0.15% benzydamine (Comparator) or 4% tulsi (Intervention) four times a day and also once half an hour before each radiotherapy session.

Clinical Trial Description

the primary outcome is the severity of oral mucositis will assess by Oral Mucositis Assessment Scale (OMAS) and secondary outcomes are pain will assess Numerical rating scale (NRS), Oral Assessment Guide (OAG), and Patient-Reported Oral Mucositis( PROMS scale) All outcomes will be recorded at baseline, and 8, 15 days ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05323058
Study type Interventional
Source Cairo University
Contact Karima AbdAllah Kamel, PhD
Phone +201014875386
Email karima.kamel@dentistry.cu.edu.eg
Status Not yet recruiting
Phase Phase 2
Start date July 2022
Completion date March 2024
View Details
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