Early Motion Following Carpal Tunnel Release

Not Applicable

Completed

• Conditions: Carpal Tunnel Syndrome
• Interventions: Behavioral: Control Group Two; Behavioral: Group One

• Registration Number: NCT00845325
• Lead Sponsor: University of Missouri-Columbia

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.

Study Timeline

• Study Start: 2008-12
• Study First Submitted: 2009-02-16
• Study First Submitted QC: 2009-02-16
• Study First Posted: 2009-02-18
• Status Verified: 2016-04
• Primary Completion: 2016-04
• Study Completion: 2016-04
• Last Update Submitted: 2016-04-27
• Last Update Posted: 2016-04-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 16

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Behavorial Control Group Two	Control Group Two	The second group will have wrist immobilization splints placed at the time surgery. The thumb and fingers will not have limited motion in this splint. Due to the splint placement, 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.
Group One	Group One	The first group (early motion) will have a bulky dressing placed at the time of surgery. They will be instructed to remove the dressing on the first postoperative day and to place a band-aid over the incision. A set of non-weight bearing "stretching" exercises will be explained on the day of surgery and instructions with diagrams sent home with the patient. They will begin these 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.

Primary Outcome Measures

Name	Time	Method
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

Trial Locations

Locations (1)

University of Missouri; 🇺🇸 Columbia, Missouri, United States