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Brain Plasticity in Carpal Tunnel Syndrome and Its Response to Acupuncture

Early Phase 1
Conditions
Carpal Tunnel Syndrome
Registration Number
NCT01345994
Lead Sponsor
Martinos Center for Biomedical Imaging
Brief Summary

This study will characterize brain plasticity in Carpal Tunnel Syndrome and will determine how this central fMRI biomarker is modulated by acupuncture. This study will also investigate the behavioral consequences of maladaptive cortical plasticity in this disease population.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  1. Male and female adults aged 20-60.

  2. History

    • Pain and/or paresthesia in median nerve distribution (i.e., numbness in some combination of digit 1, 2, 3, and the radial part of digit 4)
    • Nocturnal pain and/or paresthesia in median nerve distribution
    • Symptoms (a and b) greater than 3 months in duration
  3. Physical Exam with two of the following three findings:

    • Phalen's and Durkin's sign (positive with paresthesia in at least 1 of 3 radial digits)
    • Abnormal grip strength (greater than 2 S.D. compared to uninvolved side using an isometric hand grip device)
  4. Nerve conduction findings consistent with mild to severe CTS:

Mild CTS: Delayed distal latency of the sensory nerve conductions across the wrist (> 3.7milliseconds and/or > than 0.5 milliseconds compared to the ulnar sensory conduction) with normal motor conductions

Moderate CTS: Delayed distal latency of the sensory nerve conductions across the wrist as stated above with delayed distal latency of the motor conductions across the wrist (> 4.2 milliseconds).

Severe CTS: Delayed distal latency of the sensory nerve conductions across the wrist as stated above with greater than 50% loss of motor amplitudes (relative to unaffected side and/or normative range).

Exclusion Criteria
  1. Contraindications to MRI examination (pregnancy, pacemaker, etc. according to guidelines set by MGH NMR-Center)
  2. History of diabetes mellitus or other major cardiovascular, respiratory, or neurological illnesses.
  3. History of rheumatoid arthritis.
  4. History of wrist fracture with direct trauma to median nerve.
  5. Current usage of prescriptive opioid pain medication.
  6. Severe thenar atrophy.
  7. Nerve entrapment other than median nerve.
  8. Cervical radiculopathy or myelopathy.
  9. Generalized peripheral neuropathy.
  10. A blood dyscrasia or coagulopathy or current use of anticoagulation therapy

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Functional MRI brain responseBaseline vs. Post-Acupuncture (average 9 weeks later)

Several fMRI outcomes will be assessed including brain hyperactivity and somatotopy

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Massachusetts General Hospital

🇺🇸

Boston, Massachusetts, United States

Massachusetts General Hospital
🇺🇸Boston, Massachusetts, United States
Pia Hugus
Contact
781-391-7518
Vitaly Napadow, PhD
Principal Investigator

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