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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 therapy
K12.31
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
NameTimeMethod
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
NameTimeMethod
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