A Prospective Randomized Trial Comparing Open Reduction and Internal Fixation With Non-operative Treatment for Ulnar Shaft Fractures
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Fracture
- Sponsor
- University of Calgary
- Enrollment
- 100
- Locations
- 9
- Primary Endpoint
- Disabilities of the Arm, Shoulder and Hand (The DASH)
- Last Updated
- 3 years ago
Overview
Brief Summary
The purpose of this study is to determine if surgery using a plate and screws to fix a forearm fracture (ulnar shaft) will improve functional outcome compared to non-operative treatment out to 1 year of follow-up. It is hypothesized that in skeletally mature patients with isolated ulnar shaft fractures, the patients treated with surgery will have improved functional outcomes compared to non-surgical treatment with below-elbow cast at 1-year follow-up. This will be measured by the Disabilities of the Arm, Shoulder and Hand (DASH) scores. Secondary outcomes will include SF-36, range of motion, pain, grip strength, return to work, and time to union.
Detailed Description
Ulnar diaphyseal, or "nightstick", fractures are uncommon, but fraught with complications (Pollock et al., 1983; Grace \& Witmer, 1980, Atkin et al., 1995) and may prevent return to work (Atkin et al., 1995). 3 systematic reviews have concluded that there is insufficient evidence to guide treatment of isolated ulnar shaft fractures (Handoll \& Pearce, 2000; Mackay et al., 2000; Bhandari \& Schemitsch, 2004) and there has been no comparison between operative and non-operative management. Therefore, there is true clinical equipoise regarding optimal treatment of these injuries. The aim of this study is to determine if open reduction and internal fixation (ORIF) is more efficacious than closed reduction and below-elbow casting for 6 weeks in restoring function of the forearm and wrist. We hypothesize that in skeletally mature patients with isolated ulnar shaft fractures, ORIF will improve functional outcomes compared to non-operative treatment with below-elbow cast at 1-year follow-up. The primary objective is to compare Disabilities of the Arm, Shoulder and Hand (DASH) scores at 1-year post-injury. Secondary outcome measures include SF-36, range of motion, pain, grip strength, return to work and time to union. The study design is a multi-centre, open-label parallel randomized clinical trial. 100 skeletally mature patients with closed, extra-articular isolated ulnar diaphyseal fractures will be randomized to one of the two treatment arms. Polytrauma patients or those with pre-existing bone pathology will be excluded. Post-treatment follow-up evaluation will occur at 2, 6 and 12 weeks and at 6 and 12 months. Interim analysis will be completed by an independent Data Safety and Monitoring Committee to ensure patient safety. Radiologic displacement, angulation and time to union will be evaluated by two independent, blinded observers. Time to fracture union will be defined as bridging callus across the fracture line on 2 views. The sample size was calculated as 50 patients per group. Independent samples t-test will be used to compare the DASH and SF-36 scores and return to work. An ANOVA will be used for the DASH, SF-36 and range of motion comparison at each follow-up. There is true clinical equipoise regarding optimal treatment for isolated ulnar diaphyseal fractures, therefore, the results of this trial will provide robust evidence for clinical decision-making in the treatment of these injuries by orthopaedic surgeons.
Investigators
Paul Duffy
Division Head, Orthopaedic Trauma
University of Calgary
Eligibility Criteria
Inclusion Criteria
- •Over 16 years of age and skeletally mature
- •Subject has an isolated extra-articular ulnar diaphyseal fracture
- •Subject presents within 14 days or less between injury and study recruitment
- •Patient must be medically fit for anesthesia
- •Subject is willing and able to provide written informed consent for trial participation
- •Subject is willing and able to comply with the study protocol including return for all follow-up evaluations
- •Subject has an isolated ulnar diaphyseal fracture (AO type 22A1.1, 22A1.2, 23A1.2, 23A1.3, 22B1.1, 22B1.2) without extension to the articular surface
- •Fracture is displaced, but displacement is \<50% after closed reduction, if closed reduction is required
- •Fracture less than 30-degrees of angulation following closed reduction, if closed reduction is required
Exclusion Criteria
- •Subject has a pre-existing ipsilateral wrist injury, degenerative condition, or congenital anomaly
- •Subject has a delay in treatment greater than 14 days from time of injury
- •Subject has an active infection in the area of surgical approach
- •Subject has concomitant injury which, in the opinion of the attending surgeon, is likely to impair rehabilitation or prolong ulnar fracture healing time (another long bone fracture, ipsilateral limb injury)
- •Subject has a history of rheumatoid arthritis, fibrous dysplasia, chronic renal failure, Paget's disease, or osteopetrosis
- •Subject has a high risk of death from surgery (ASA physical status Class V)
- •Subject is likely unable to maintain follow-up (no fixed address, plans to move out of town in the next year, states unable to comply with protocol, etc)
- •Subject has cognitive impairment or language difficulties that would impeded the valid completion of questionnaires
- •Subject is pregnant
- •Subject is a prisoner, currently detained
Outcomes
Primary Outcomes
Disabilities of the Arm, Shoulder and Hand (The DASH)
Time Frame: 1 year
30-item, self-reported questionnaire that evaluates function of the affected upper extremity and will reveal the impact of the forearm injury on the function of the entire limb
Secondary Outcomes
- Range of Motion(2 weeks, 6 weeks, 12 weeks, 6 months, 12 months)
- Radiologic outcome - time to union (fracture healing)(baseline, 2 weeks, 6 weeks, 12 weeks, 6 months, 12 months)
- DASH score(baseline, 2 weeks, 6 weeks, 12 weeks, 6 months, 12 months)
- Grip Strength(6 weeks, 12 weeks, 6 months, 12 months)
- SF-36(baseline, 2 weeks, 6 weeks, 12 weeks, 6 months, 12 months)
- Pain Visual Analogue Score(baseline, 2 weeks, 6 weeks, 12 weeks, 6 months, 12 months)