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NCT01394822 Clinical Trial

Neuromuscular Ultrasound for Focal Neuropathies

Carpal Tunnel Syndrome Clinical Trial

Official title:
Neuromuscular Ultrasound for Focal Neuropathies

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01394822
Other study ID # NINDS-K23NS062892
Secondary ID
Status Completed
Phase N/A
First received July 13, 2011
Last updated November 2, 2017
Start date September 2011
Est. completion date March 2014

Study information
Verified date December 2014
Source Wake Forest University Health Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine if a new diagnostic technique, called neuromuscular ultrasound, can improve our ability to diagnose focal nerve disease.

Recruitment information / eligibility
Status Completed
Enrollment 120
Est. completion date March 2014
Est. primary completion date March 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Electrodiagnostic finding of focal nerve disease

- Age 18 and older

Exclusion Criteria:

- Skin lesions preventing ultrasound

- Known ultrasound gel allergy

- Unable to complete 6 months of follow-up

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Wake Forest Baptist Medical Center Winston-Salem North Carolina

Sponsors (1)
Lead Sponsor Collaborator
Wake Forest University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Overall Neuropathy Sum Score Neuropathy specific scale 6 months
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