Carpal Tunnel Syndrome Clinical Trial
Official title:
Corticosteroid Injection as a Predictor of Outcome in Carpal Tunnel Release
Verified date | March 2011 |
Source | Vanderbilt University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Observational |
This study will investigate whether symptomatic improvement following carpal tunnel
corticosteroid injection can be correlated to symptomatic improvement following carpal
tunnel release and therefore serve as a prognostic indicator.
Clinical question: Does response to corticosteroid injection in CTS predict outcomes of
surgical treatment?
Secondary Questions:
1. Can we confirm previous retrospectively collected data that a certain percentage of
conservatively managed patients with steroid injection will avoid surgery, and that
patients who undergo surgery will have better outcomes than those who do not.
2. Are there differences between worker's compensation and non-worker's compensation
patients with regard to the primary clinical question?
3. What are Carpal Tunnel Release outcomes for the subset of patients with negative
electrophysiologic studies?
4. What are the outcomes of patients who undergo carpal tunnel release vs. those who
choose not to undergo carpal tunnel release?
A prospective cohort design study is the appropriate study design in order to measure the
association between a predictor (response to injection) and outcome (response to surgery).
Status | Terminated |
Enrollment | 200 |
Est. completion date | March 2011 |
Est. primary completion date | March 2011 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients with a clinical diagnosis of carpal tunnel syndrome - English speaking patients only Exclusion Criteria: - Patients less than 18 years old - Patients who are pregnant by patient report or intending to become pregnant during the study - Patients unwilling or unable to return for follow-up visits prescribed by the study protocol. - Patients who qualify for inclusion in the study, but refuse to participate. - Patients with evidence of thenar atrophy on exam - Patients with a diagnosis of peripheral neuropathy or other neuropathy. - Patients with previous ipsilateral carpal tunnel injection or release. |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | Vanderbilt Hand & Upper Extremity Center | Nashville | Tennessee |
Lead Sponsor | Collaborator |
---|---|
Vanderbilt University |
United States,
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