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Ultrasonographic Measurements of the Median Nerve Before and After Splinting for Carpal Tunnel Syndrome

NCT02038205 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 213

Last updated 2017-02-23

No results posted yet for this study

Summary

A prospective cohort follow-up study design is undertaken. Both males and females with mild to moderate carpal tunnel syndrome will receive standard-of-care wrist splint for 6 weeks and undergo follow up studies for data collection. Controls will also be seen for a one time visit.

Conditions

  • Carpal Tunnel Syndrome

Sponsors & Collaborators

  • University of California, Davis

    lead OTHER

Principal Investigators

  • Nanette Joyce, DO · University of California, Davis

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-01-31
Primary Completion
2016-11-30
Completion
2016-11-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02038205 on ClinicalTrials.gov