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Wrist Denervation Vs Exercise in Wrist Osteoarthritis

Not Applicable
Recruiting
Conditions
Osteoarthritis Wrist
Interventions
Behavioral: Self-managed exercise therapy program
Procedure: Partial wrist denervation
Registration Number
NCT06098586
Lead Sponsor
Karolinska Institutet
Brief Summary

A randomized controlled trial comparing partial wrist denervation to a self-managed exercise therapy program in 140 patients with wrist osteoarthritis.

Detailed Description

Backgroud:

High quality evidence regarding the effectiveness of non-operative and operative treatments in wrist osteoarthritis are lacking.

Aim:

To analyze:

1. Does partial wrist denervation and self-managed exercise therapy improve patient-reported outcomes, pain, grip strength and range of motion (ROM) in wrist OA?

2. Is any of the two treatment concepts partial wrist denervation and self-managed exercise therapy more efficient than the other in terms of patient-reported outcomes, pain relief, grip strength and range of motion?

Method:

A multicenter parallel group, two-arm, randomized, controlled, assessor blinded, trial of 140 patients. The study is conducted at the departments of hand surgery at Södersjukhuset Stockholm and Malmö University hospital.

Group1:

Self-managed exercise therapy program containing:

* Patient education:

* Exercise therapy program:

The exercise therapy program is designed by Sara Larsson (physiotherapist at the Department of hand surgery in Malmö, Sweden), influenced by previous studies on wrist stability and proprioception. Focus is on functional re-learning and strengthening of the musculoskeletal system with the aim to create a stable wrist that can be used in a pain-free manner in activities of daily living. The program consists of neuromuscular exercises that focus on coordination, wrist stability and strength.

Group 2:

Surgery will be performed under local anesthesia (+ blood-less field or wide-awake local anesthesia no torniquet (WALANT) according to the surgeon's preference) through a single dorsal incision. AIN and PIN neurectomy will be performed as described by Berger (Berger, 1998).

Primary outcome:

Patient Rated Wrist Evaluation (PRWE) score (0-100) (MacDermid et al., 1998) 12 months after intervention.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
140
Inclusion Criteria
  • Age ≥ 18 years.
  • Chronic wrist pain (≥6 months) due to Scapholunate advanced collapse (SLAC) / Scaphoid non-union advanced collapse (SNAC) grade 1-3 osteoarthritis.
  • Radiological signs of osteoarthritis on posteroanterior and lateral radiograph.
Exclusion Criteria
  • Previous PIN or AIN neurectomy.
  • Rheumatoid arthritis or other chronic inflammatory arthritis.
  • Symptomatic osteoarthritis in the distal radio-ulnar (DRU), Scapho-trapezio-trapezoid (STT) or thumb carpometacarpal (CMC) joints.
  • Ongoing infection.
  • Inability to co-operate with the follow-up protocol.
  • Systemic or intra-articular glucocorticoids or intraarticular PRP or Hyaluronic acid injections in the affected joint within 3 months prior to enrollment.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Self-managed exercise therapy programSelf-managed exercise therapy programExercise program focusing on functional re-learning and strengthening of the musculoskeletal system with the aim to create a stable wrist that can be used in a pain-free manner in activities of daily living.
Partial wrist denervationPartial wrist denervationAIN and PIN neurectomy through a dorsal approach as described by Berger (Berger, 1998).
Primary Outcome Measures
NameTimeMethod
PRWE6 months

Patient Rated Wrist Evaluation (PRWE) score (0-100 (high score worse outcome)) (MacDermid et al., 1998)

Secondary Outcome Measures
NameTimeMethod
PRWE5 years

Patient Rated Wrist Evaluation (PRWE) score (0-100 (high score worse outcome)) (MacDermid et al., 1998)

Pain NRS5 years

Pain at rest and on load measured by a Numerical Rating Scale (NRS, 0-100 (higher score worse outcome) (Salaffi et al 2004)

EQ5D5 years

EQ-5D-5L (0-1 (higher score better outcome)) (Brooks, 1996)

GROC5 years

Global rating of change (GROC, -5-+5, higher score better outcome)

Pain catastrophizing5 years

PCS (Pain catastrophizing scale, 0-52, higher score worse outcome) (Sullivan et al, 1995)

ROM5 years

Range of motion (ROM) of the wrist.

Grip5 years

Grip strength (Jamar).

Complications5 years

Complications related to treatment

Radiology5 years

Radiological grade of osteoarthritis 5 years after inclusion compared to baseline.

Cost12 months

Differences in direct costs associated with treatment and indirect costs.

sick leave12 months

length of sick leave

work12 months

ability to return to previous work

Survival5 years

Success of the intervention, i.e no additional surgery during the study period due to lack of treatment effect or recurrence of symptoms.

Trial Locations

Locations (2)

Department of hand surgery, Malmo university hospital

🇸🇪

Malmo, Sweden

Department of hand handsurgery, Södersjukhuset

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Stockholm, Sweden

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