Evaluating the pain relieving effects of Non-Thermal CO2 Laser Therapy (NTCLT) on chemotherapy induced oral mucositis
Phase 2
- Conditions
- Chemotherapy-induced oral mucositis.Oral mucositis (ulcerative) due to antineoplastic therapyK12.31
- Registration Number
- IRCT20220220054073N1
- Lead Sponsor
- Iran National Science Foundation (INSF)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Chemotherapy-induced oral mucositis with grade 1-4 according to the WHO classification index
The minimum literacy to read and write and filling the forms
Providing written informed consent after the physician's explanation about the treatment method
Exclusion Criteria
Pregnancy
Breastfeeding
History of Photo sensitivity or use of photo sensitizing drugs
Head and neck radiotherapy
Taking narcotic painkillers
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method on-contact (Non-stimulate) pain score. Timepoint: before laser irradiation, immediately after laser irradiation, 4 hours, 8 hours after laser irradiation and then daily until the seventh day. Method of measurement: (Visual analogue scale) VAS.;Contact pain score. Timepoint: before laser irradiation, immediately after laser irradiation, 4 hours, 8 hours after laser irradiation and then daily until the seventh day. Method of measurement: (Visual analogue scale) VAS.
- Secondary Outcome Measures
Name Time Method