Evaluation of low level laser effect in prevention of oral mucositis in patients with cancer
Not Applicable
- Conditions
- Chemotherapy Induced Mucositis.Other and unspecified lesions of oral mucosa
- Registration Number
- IRCT138811033133N1
- Lead Sponsor
- Zahedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
patients with Karnofsky Performance status equal or more than 60, hope for life more than 6 months, absence of previous chemotherapy toxicity, WBC count equal or more than 1500, platelet count equal or more than 100000 /ml, patients who sign informed consent
Exclusion criteria: Simultaneous radio therapy with chemotherapy or previous radiotherapy in head and neck, head and neck surgery cause of malignancy, Denture or something like that, Pregnancy, infection
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Oral Mucositis. Timepoint: Every 14 days. Method of measurement: WHO standard scale( 0-4).
- Secondary Outcome Measures
Name Time Method Xerostomia. Timepoint: Every 14 days. Method of measurement: LENT SOMA scale (1-4).;Pain. Timepoint: Every 14 days. Method of measurement: VAS.