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Early Motion Following Carpal Tunnel Release

Early Motion Following Carpal Tunnel Release, a Randomized Control Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00845325
Enrollment
16
Registered
2009-02-18
Start date
2008-12-31
Completion date
2016-04-30
Last updated
2016-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carpal Tunnel Syndrome

Keywords

Carpal tunnel release, Rehabilitation, Early motion

Brief summary

To objectively and subjectively assess two modes of commonly employed rehabilitation and confirm a superior method to treat patients following carpal tunnel release. One of the problems following carpal tunnel release (CTR) for carpal tunnel syndrome, and all hand surgeries, is the debilitation in the postoperative period. This relates to muscle atrophy and joint stiffness due to immobilization or relative inactivity in the postoperative period. Specifically, patients suffer increased days off from work, lost wages, and difficulties with activities of daily living affecting the patient and society at large. CTR is a very common procedure in hand surgery making it easy to study and important to optimize the postoperative care.

Detailed description

The surgical procedure, carpal tunnel release, will be performed in a standard open fashion. In a random fashion, the patients will be placed into either of two rehabilitation groups following CTR with specifically different postoperative instructions after the procedure.

Interventions

BEHAVIORALGroup One

They will begin exercises on the day after surgery and perform them three times daily for two weeks. The patients will have no restrictions concerning activity or return to work.

BEHAVIORALControl Group Two

The patients will be restricted from using that hand during its implementation. One week following surgery the splint will be removed and the patient will be instructed to begin activity without restriction.

Sponsors

University of Missouri-Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of carpal tunnel syndrome * Recommended for carpal tunnel release

Exclusion criteria

* Severe thenar weakness * proximal neuropathy of the same arm. * generalized peripheral neuropathy * active psychiatric disorder * chronic renal failure require dialysis * reflex sympathetic dystrophy * previous injury of affected wrist or median nerve * simultaneous ipsilateral upper extremity surgery * carpal tunnel syndrome with acute injury

Design outcomes

Primary

MeasureTime frame
days to return to activities of daily living, return to work, grip strength, pinch strength, digital sensibility, subjective pain control, number of pain pills used, grading of success,and any complications encountered.1 week, 3 weeks, 3 months, and 1 year postoperatively

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026