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Recruiting NCT05818241

NCT05818241 Satisfaction and Recovery After Distal Radius Fracture

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Clinical Trial Summary
NCT ID NCT05818241
Status Recruiting
Phase
Sponsor Sahlgrenska University Hospital
Condition Distal Radius Fracture
Study Type OBSERVATIONAL
Enrollment 300 participants
Start Date 2023-01-12
Primary Completion 2027-01-31

Trial Parameters

Condition Distal Radius Fracture
Sponsor Sahlgrenska University Hospital
Study Type OBSERVATIONAL
Phase N/A
Enrollment 300
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2023-01-12
Completion 2027-01-31
Interventions
Treatment of fracture by forearm castSurgical treatment of fracture

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Brief Summary

Distal radius fracture is the most common fracture in Sweden, but little is known about the patient's experience of pain and hand function during the first three months after the injury. This observational study will provide detailed information on a daily basis regarding pain, use of analgesic drugs, use of splints and hand function as measured weekly by a condition-specific questionnaire.

Eligibility Criteria

Inclusion Criteria: * Unilateral distal radius fractures in patients without any other significant injuries regardless of ligament injuries and ulnar fractures. * Signed written consent Exclusion Criteria: * Compound injuries * Open fractures * Patients with post traumatic function deficits at any level in the affected arm prior to the distal radius fracture. * Patients with function deficits in the affected arm due to other medical conditions (e.g. Parkinsons disease, Rheumatoid Arthritis) * Reduced mental capacity (e.g. dementia, substance abuse)

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