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Evaluation of RTMS on Phantom Limb Pai

Not Applicable
Recruiting
Conditions
amputee patients with phantom limb pain.
Phantom limb syndrome without pain
Registration Number
IRCT20180619040148N1
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
10
Inclusion Criteria

Amputee Patients with phantom pain due to cancer
Resistant to treatment with gabapentin or pregabalin dosage after one month
Pass at least three months from the time of amputation

Exclusion Criteria

history of seizure
spastic lesion in the brain
Non-symmetric nerve exam with suspicion of central lesion
Inability to complete the pain questionnaire
vascular stent in the heart arteries or head and neck
metal piece in the body

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain score. Timepoint: Measurement of pain score before the intervention, immediately after each treatment session, one month and six months after the end of treatment. Method of measurement: McGill Pain score questioner.
Secondary Outcome Measures
NameTimeMethod
Depression score. Timepoint: Measurement of depression score before the intervention, immediately after each treatment session, one month and six months after the end of treatment. Method of measurement: Beck Depression Inventory-II.
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