Early Motion Following Carpal Tunnel Release

University of Missouri (MU)

Status: Completed

Conditions: Carpal Tunnel Syndrome

Treatments: Behavioral: Group One; Behavioral: Control Group Two

Study type: Interventional

Funder types: Other

Identifiers

NCT00845325

1108957

Details and patient eligibility

About

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.

Full 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.

Enrollment: 16 patients

Sex: All

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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16 participants in 2 patient groups

Group One

Active Comparator group

Description:

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.

Treatment:

Behavioral: Group One

Behavorial Control Group Two

Other group

Description:

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.

Treatment:

Behavioral: Control Group Two