Intraneural Facilitation as a Treatment for Carpal Tunnel Syndrome
Completed · Not applicable · Has a placebo group
Conditions studied: Carpal Tunnel Syndrome
In brief
We hypothesize that a standard course of INF can result in significant improvement in CTS as measured by clinical, electrodiagnostic, or ultrasound measures.
Key facts
- Study ID
- NCT03205683
- Run by
- Loma Linda University
- People needed
- 10
- Starts
- 2018-01-29
- Expected to finish
- 2019-02-22
- Last updated by the study team
- 2019-09-10
Who can join
Age: 19 and older, up to 74. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Patients referred to the LLUH Neurology Electrodiagnostic Laboratory with electrodiagnostic and clinical evidence of CTS (uni- or bilateral)
- Ages >18 and < 75 (irrespective of gender)
- Current use of splints as long as the frequency of treatment is unaltered and onset of use is > 1 week in duration
You may not qualify if…
- Prior carpal tunnel release > 2 years ago
- The presence of any condition that would prevent NCS from accurately diagnosing CTS (e.g., hereditary polyneuropathy or acquired demyelinating polyneuropathy)
- Workman's Compensation cases
- Pregnancy
- Undergoing conservative or surgical/injection therapy (physical or occupational therapy, injections)
- Clinically silent CTS in face of positive electrodiagnostic results
- Sufficiently severe clinical symptoms that warrant more aggressive therapy i.e., carpal injections or release
- Any confounding medical condition that the investigator deems may adversely affect subject participation or outcomes
Where it is running
- Loma Linda University Health — Loma Linda, California, United States
Full record on ClinicalTrials.gov
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