Olecranon Fracture Clinical Trial
Official title:
Randomzied Controlled Trial Comparing Tension Band Wiring and Plate Fixation in the Treatment of Olecranon Fractures in Adults
Verified date | September 2021 |
Source | Oslo University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The incidence of olecranon fractures is 12 per 100.000. Traditionally, isolated olecranon fractures have been treated with tension band wiring (TBW). There is a trend towards increased use of plate fixation, though TBW has yielded good and comparable patient reported outcomes. The latter method is substantially cost-effective, but higher complication reports have been reported. There are only two randomized controlled trials comparing TBW and plate fixation, and the literature is inconclusive in which fixation method is preferable in the treatment of olecranon fractures. In this multi-center trial, adult patients (18-75 years) with isolated olecranon fractures will be randomized to either TBW or plate fixation.
Status | Active, not recruiting |
Enrollment | 200 |
Est. completion date | September 1, 2022 |
Est. primary completion date | August 1, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: - Patients between the age of 18 and 75 years with an olecranon fracture Mayo type IIA or IIB will be eligible for inclusion. Exclusion Criteria: - Patients younger than 18 or older than 75 years of age. - Unable to receive oral and written information. - Concomitant fracture in the injured extremity. - When the olecranon fracture extends distal to the coronoid process. - Previous injury or illness in the injured upper extremity with permanent reduced elbow function. |
Country | Name | City | State |
---|---|---|---|
Norway | Oslo University Hospital | Oslo |
Lead Sponsor | Collaborator |
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Oslo University Hospital |
Norway,
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* Note: There are 15 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The Quick Disability of the Arm, Shoulder and Hand Outcome Measure (QuickDASH) | The QuickDASH questionnaire evaluates difficulty performing specific tasks and symptoms, social and work function, sleep and confidence. Scaling is ranked from 0 indicating least disability to 100 indicating most disability. | 12 months | |
Secondary | Mayo Elbow Performance Score (MEPS) | MEPS is the primary outcome parameter. MEPS consist of four categories evaluating pain, range of motion, stability and function.6 The scale ranges from 0 to 100, with higher score indicating better outcome. Pain is weighed highest of the 4 variables. Patient outcome can be categorized into excellent (MEPS > 90), good (MEPS 75-90), fair (MEPS 60-74) and poor (MEPS < 60). | 12 months | |
Secondary | Grip strength | A hand dynamometer will be used to measure grip strength in both hands | 12 months | |
Secondary | Range of motion (ROM) | A goniometer will be used to register ROM in elbow flexion, extension and rotation. | 12 months | |
Secondary | The EuroQol five dimensions questionnaire (EQ-5D-5L) | Health status is measures health status/quality of life into one of five levels for the five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. The data is computed to a number (EQ-Index) ranging from 0-1.00, where 1.00 is the best possible outcome, and negative values describe a status theoretically worse than being dead. In addition, the patients score their overall life quality on a vertical line, directly measured in millimeters as EQ-VAS score (0-100, 100 best). | 12 months | |
Secondary | Satisfaction with elbow function | An individual satisfaction assessment will be recorded using a visual analogue scale (VAS) of elbow function at follow-up. Zero indicating minimal satisfaction, and 100 indicating maximal satisfaction. | 12 months | |
Secondary | Subjective pain on a scale from 0 (no pain) to 100. | An individual pain assessment will be recorded using a visual analogue scale (VAS) of elbow pain at follow-up. Zero indicating no pain, and 100 indicating maximal pain. | 12 months | |
Secondary | Complications | The patient charts will be reviewed for reports of neurological deficiencies, and an examination of neurologic function will be performed at follow-up. Scar problems, infections, non- and mal-unions and hardware issues will also be reviewed and reexamined. The definition of infection is:
Less serious infection: Superficial wound infection with sign of skin inflammation and/or positive bacterial culture, without the need for secondary surgery, i.e. surgical debridement. Serious infection: Any postoperative wound infection or sign of deep infection that require secondary surgery. |
12 months | |
Secondary | Hardware removal | Rates of planned and performed hardware removal. | 12 months | |
Secondary | Radiographic evaluation | Radiographs and computer tomographic (CT) scan will be obtained pre- and postoperatively for optimal classification. Radiographs will also be obtained at six weeks, 3 months, and 12 months. Plain x-rays will include true antero-posterior and lateral projections. The fracture pattern will be classified according to the Mayo classification and Schatzker classification. All radiographs will be reviewed and classified by two senior orthopedic trauma surgeons. Assessment of union and non-union will be assessed and recorded. Displacement of the fracture fragments is to be registered in millimeters at the level of the joint. The joint congruency following surgery and at the following radiographs will be evaluated. Osteoarthritis will be classified according to the system of Broberg and Morrey. Heterotopic ossification will be classified according to Hastings and Graham. | 12 months |
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