Ultrasonographic Measurements of the Median Nerve Before and After Splinting for Carpal Tunnel Syndrome
Status: | Completed |
---|---|
Conditions: | Orthopedic |
Therapuetic Areas: | Orthopedics / Podiatry |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/24/2017 |
Start Date: | January 2014 |
End Date: | November 2016 |
High Resolution Ultrasonographic Measurements of the Median Nerve Before and After Wrist Splinting for Carpal Tunnel Syndrome
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.
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.
Inclusion Criteria:
- 18 years or older and;
- Diagnosis of mild to moderate CTS with median motor latency at 8 cm is greater than
4.5 milliseconds or Combined Sensory Index > 0.9 where first line therapy is
indicated to include nocturnal wrist bracing
- Control subjects without symptoms of carpal tunnel syndrome.
Exclusion Criteria:
- Evidence of severe CTS as seen with electromyographic changes in the body of the
muscle
- Untreated hypothyroidism, Rheumatologic disorders
- Diagnosed Severe CTS or Chronic symptoms of carpal tunnel, greater than 1 year, this
includes wasting of the hand muscles
- Undergoing or previously treated for carpal tunnel on affected side. This includes
surgery (carpal tunnel release), corticosteroid injections, bracing within the last 3
months while wearing the brace consistently every night, or any other intervention.
- Currently pregnant or < 3 months post partum
- History of wrist, hand fracture or severe trauma to affected hand and/or wrist
- Known tumor, mass or deformity of the hand/wrist
- Inflammatory articular disease of the joints or tendons Existing cervical
radiculopathy or previous surgeries to the neck for radicular symptoms
- History of electrodiagnostic evidence of generalized polyneuropathy or evidence of
denervation
- Diagnosed neuromuscular disorders which may complicate CTS diagnosis
- Implanted electronic device (pacemaker, intrathecal pump/stimulator)
- Any illness that makes it unsafe for the patient to participate in the study
- Not fluent in English as NeuroQOL and other subjective information is limited to the
English language interpretation
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