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Treatment of Carpal Tunnel Syndrome With Dynamic Splinting

NCT00558116 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2008-05-13

No results posted yet for this study

Summary

The Purpose of this study is to examine the effect of using the Carpal Tunnel Dynasplint® System on patients diagnosed with CTS in a randomized, controlled, cross-over study.

Conditions

  • Carpal Tunnel Syndrome

Interventions

DEVICE

Dynamic splinting

The Dynasplint carpal tunnel device will be worn for 30 minutes, twice daily, for 60 consecutive days.

Sponsors & Collaborators

  • Dynasplint Systems, Inc.

    collaborator INDUSTRY

  • Advanced Centers for Orthopaedic Surgery and Sports Medicine

    lead OTHER

Principal Investigators

  • Stacey H Berner, MD · Advanced Centers for Orthopaedic Surgery and Sports Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-05-31
Primary Completion
2008-11-30
Completion
2008-12-31

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 NCT00558116 on ClinicalTrials.gov