Immediate Mobilization Versus 2 Weeks Cast Immobilization After Distal Radius Fracture Treated With Volar Locking Plate
- Conditions
- Distal Radius Fracture
- Interventions
- Other: Immediate mobilizationOther: Cast treatmentProcedure: Volar plating
- Registration Number
- NCT05150925
- Lead Sponsor
- Tampere University Hospital
- Brief Summary
The aim of this study is to analyze total lenght of the sick leace and functional outcome (PRWE) at 2 months between 2 weeks casting and immediate mobilization following volar plating for a DRF.
- Detailed Description
This study is a prospective, randomized, controlled trial. The aim of this study will be to compare the early postoperative outcomes of the patients enrolled in the early mobilization with those patients in post-operative 2-week casting following volar plating for a DRF. Co-primary outcome in this study will be the total lenght of sick leave and Patient-Rated Wrist Evaluation (PRWE) 2 months after the operation.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 240
- Intra- or extra articular DRF (Colles, Smith, Volar barton)
- operative treatment justified
- Refusal to participate in the study
- Open fracture with a severity greater than Gustilo grade 1
- Patient aged less than 18 or over 65
- Patient does not understand written or spoken guidance in local languages
- Pathological fracture
- Previous fracture in the same wrist or forearm in the last 10 years, that has led to impairment of function
- Ipsilateral fracture in upper extremity
- Associated fractures of the ulna (except fractures of the PSU)
- Polytrauma
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description 2 weeks cast immobilization after distal radius fracture treated with volar locking plate Volar plating - Immediate mobilization after distal radius fracture treated with volar locking plate Immediate mobilization - 2 weeks cast immobilization after distal radius fracture treated with volar locking plate Cast treatment - Immediate mobilization after distal radius fracture treated with volar locking plate Volar plating -
- Primary Outcome Measures
Name Time Method Patient-rated wrist evaluation questionnaire 2 months The PRWE is a 15-item questionnaire designed to measure wrist pain and disability in daily activities. It ranges from 100 (worst) to 0 (best). It consists of 2 subscales. Pain subscale contains 5 items. Function subscale contains total 10 items which are further divided into 2 sections: specific activities (having 6 items) and usual activities.
Total lenght of the sick leave 12 months Total number of days of work during the 1 year study period
- Secondary Outcome Measures
Name Time Method Patient-rated wrist evaluation questionnaire 12 months The PRWE is a 15-item questionnaire designed to measure wrist pain and disability in daily activities. It ranges from 100 (worst) to 0 (best). It consists of 2 subscales. Pain subscale contains 5 items. Function subscale contains total 10 items which are further divided into 2 sections: specific activities (having 6 items) and usual activities.
Return to work 12 months Patient is asked if he or she has returned to the previous work. If no patient is asked is he or she Still on sick leave, partial sick leave or returned to other work.
Complications 12 months Any surgery related complication: wound dehiscence, deep infection, flexor tendon rupture, nerve injury, mechanical complications, nonunion, malunion, complex regional pain syndrome
Work capacity 12 months The participants will be asked to rate their working capacity on a numerical scale from 0 to 10, with "0" being not able to work at all and "10" being the ability to work at its best.
Visual analogue pain scale 12 months Overall pain during last 7 days in a scale from 0 to 100 (worst)
Self-perceived working ability 12 months Patient is asked to rate his os her working ability using two scales: NRS from 0 (fully disabled) to 10 (best capability) and ordinally (fully capable, partially capable, fully disabled).
Patient-acceptable symptom state 12 months Patient satisfaction will be measured using the patient-acceptable symptom state (PASS).The questionnaires will include the following questions: Would you be willing to take the same treatment again if the treatment result was as it is now? (Yes/No) Considering all the different ways your injury is affecting you, if you would remain in this state, do you feel that your current state is satisfactory (Yes/No)?
Trial Locations
- Locations (2)
Teemu Karjalainen
🇫🇮Jyväskylä, Finland
Laura Kärnä
🇫🇮Tampere, Finland