Evaluation of N-Acetyl Cysteine mouthwash in preventing the occurrence of chemotherapy-induced oral mucositis
Phase 3
Recruiting
- Conditions
- chemotherapy-induced oral mucositis.K12.3Oral mucositis (ulcerative)
- Registration Number
- IRCT20220712055439N1
- Lead Sponsor
- Mazandaran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 68
Inclusion Criteria
Cancer patients undergoing chemotherapy for the first time
Patients who do not have other systemic diseases
Exclusion Criteria
Patients who have other systemic diseases
Taking antibiotics, drugs, cigarettes and other mouthwashes
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of Mucositis. Timepoint: During the 14 days of the study (from the first day to the fourteenth day after the start of chemotherapy). Method of measurement: The oral diseases specialist performs the examination based on the classification of the oral mucositis index and records the results in the classification.
- Secondary Outcome Measures
Name Time Method