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effect of laser therapy on symptoms of chemotherapy induced neuropathy

Not Applicable
Recruiting
Conditions
hemotherapy-induced neuropathy.
Registration Number
IRCT20240107060640N1
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

Cancer patients who took the following chemotherapy drugs during treatment: 1. Platinum compounds 2. Vinca alkaloids3. Bortezomib 4. Taxans 5. Fluorouracil6. Thalidomide, lenalidomide
At least 6 months have passed since the end of the patient's chemotherapy.
The signs and symptoms of the disease have caused a decrease in the patient's quality of life.
Filling out the Toronto questionnaire

Exclusion Criteria

Entry into the study is subject to the absence of neuropathy due to other causes of neuropathy, including diabetes, radiculopathies, hereditary and acquired neuropathies, which can be verified at the beginning of the study through history and NCV.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
creasing the score obtained in the Toronto questionnaire based on history and examination and improvement of nerve conduction. Timepoint: History and examination and nerve conduction test at the beginning of the study and two weeks after the end of laser therapy. Method of measurement: Oronto neuropathy questionnaire and nerve conduction test.
Secondary Outcome Measures
NameTimeMethod
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