effect of propolis on oral mucositis resulting from radiotherapy

Phase 3

• Conditions: Oral mucositis (ulcerative) due to radiation.; Oral mucositis (ulcerative) due to radiation; K12.33

• Registration Number: IRCT20161024030475N4
• Lead Sponsor: Tehran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 October 2019

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 72

Inclusion Criteria

head and neck cancer
requiring radiotherapy
mucositis

Exclusion Criteria

weak patients' cooperation
allergic reaction to propolis

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Mucositis severity and percentage. Timepoint: baseline / 2 weeks after completing radiotherapy. Method of measurement: based on WHO.;Incidence of mucositis. Timepoint: baseline. Method of measurement: starts 1-2 weeks after radiotherapy and is determined by clinical assessment.;TNF in saliva. Timepoint: baseline/ 2 weeks after completing radiotherapy. Method of measurement: ELISA Kis.