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Effect of Gallium-arsenide low power laser on pain after tympanomastoidectomy

Not Applicable
Recruiting
Conditions
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Chronic serous otitis media
H65.2
Registration Number
IRCT20080831001138N28
Lead Sponsor
Rasht University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
128
Inclusion Criteria

Patients 20 to 60 years with postoperative tympanomastoidectomy headache

Exclusion Criteria

Patients with bell's paralysis
Patients with various types of neuralgia
Patients with corticosteroids drug consumption
Patients with various types of tumors and malignancies

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Evaluation of pain intensity before laser therapy, in the first session after laser therapy, in the fifth session of laser therapy sessions and after the completion of laser therapy sessions are performed. In the end, the patient's pain relief ratio is measured from the beginning of the study to the end of all sessions. Method of measurement: The visual analog scale (VAS) questionnaire and Headache section from disability neck disability index (NDI).
Secondary Outcome Measures
NameTimeMethod
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