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Clinical Trials/NCT03033173
NCT03033173
Completed
Not Applicable

Ratio of the Cross Sectional Area of Median Nerve to Ulnar Nerve in Diagnosing Carpal Tunnel Syndrome

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
An Innovative Diagnostic Method for Carpal Tunnel Syndrome
Sponsor
Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation
Enrollment
74
Primary Endpoint
Sonographical findings between hands with CTS and healthy hands
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

An innovative diagnostic ultrasound method for carpal tunnel syndrome was proposed and compared between carpal tunnel syndrome patients and healthy volunteers.

Registry
clinicaltrials.gov
Start Date
January 2013
End Date
December 2014
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • CTS patients were required to have subjective symptoms of numbness, tingling pain, or dysesthesia over the median nerve innervated area of the involved hand.
  • Patients should have positive response in either Tinel's test or Phalen's test during physical examination
  • Evidence of median neuropathy at wrist level in NCS.
  • Control subjects should have neither symptoms nor signs of CTS along with no abnormal findings in electrodiagnostic study of the median nerve and the ulnar nerve across the wrist joint.

Exclusion Criteria

  • Age younger than 20 years old
  • Electrodiagnostic evidence of ulnar neuropathy at the wrist level
  • Previous trauma or surgery history of hand
  • Medical history of hypothyroidism, diabetes mellitus, uremia, rheumatoid arthritis, amyloidosis, and acromegaly
  • Pregnancy

Outcomes

Primary Outcomes

Sonographical findings between hands with CTS and healthy hands

Time Frame: Within one week after ultrasound examination

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