Surgical Treatment Versus Non-surgical Treatment of Ulnar Fractures

A Prospective Randomized Trial Comparing Open Reduction and Internal Fixation With Non-operative Treatment for Ulnar Shaft Fractures

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.

Study Overview

• Status: Active, not recruiting
• Conditions: Trauma; Surgery; Fracture; Orthopedic; Ulna Fracture
• Intervention / Treatment: Procedure: Open reduction and internal fixation; Procedure: Closed reduction and short-arm cast

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.

• Study Type: Interventional
• Enrollment (Actual): 100
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Canada
  • Alberta
    • Calgary, Alberta, Canada, T2N 2T9
      • Dr. Paul J Duffy
  • British Columbia
    • New Westminster, British Columbia, Canada
      • Royal Columbian Hospital
    • Vancouver, British Columbia, Canada
      • Vancouver General Hospital
  • Newfoundland and Labrador
    • St. John's, Newfoundland and Labrador, Canada
      • Memorial University
  • Nova Scotia
    • Halifax, Nova Scotia, Canada
      • Queen Elizabeth II Hospital
  • Ontario
    • Ottawa, Ontario, Canada
      • Ottawa Hospital
    • Toronto, Ontario, Canada
      • St. Michael's Hospital
  • Quebec
    • Montreal, Quebec, Canada
      • McGill University Health Centre
• United Kingdom
  • Bristol, United Kingdom
    • North Bristol NHS Trust

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 16 years and older (Child, Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

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
• Subject has an articular fracture (AO Type 23A1.1, 23B or 23C)
• Open ulnar fracture (any Gustilo grade)
• Segmental fracture
• Fractures within 2 cm of the distal radioulnar joint (AO 23A1.1)
• Fracture of the proximal 1/3 of the ulnar shaft (i.e. Monteggia fracture pattern, AO Type 21A, 22A1.3, 22B1.3)
• Pathologic fracture

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Surgery; Isolated ulnar shaft fractures will be treated with open reduction and internal fixation using a limited contact dynamic compression (LC-DC) plate with screws. These will remain at the fracture site for the lifetime of the patient.	Procedure: Open reduction and internal fixation; Patients will undergo surgery for open reduction of the fracture and internal fixation with an LC-DC plate and screw fixation.; Other Names: Limited contact dynamic compression plate (LC-DC) with screw fixation
Active Comparator: Short arm cast; Those individuals randomized to the non-operative treatment group will be treated with a closed reduction and short-arm (below-elbow) cast.	Procedure: Closed reduction and short-arm cast; Patient will undergo a closed reduction and be placed in a short-arm (below-elbow) cast for 6 weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Disabilities of the Arm, Shoulder and Hand (The DASH)	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	1 year

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Range of Motion	An evaluation of the range of motion about the wrist and the elbow for both the affected limb and the unaffected limb post-treatment. It will be evaluated starting at 2 weeks for the surgical group and at 6 weeks for the below-elbow cast group.	2 weeks, 6 weeks, 12 weeks, 6 months, 12 months
Grip Strength	An evaluation of the grip strength for both the affected limb and the unaffected limb post-treatment.	6 weeks, 12 weeks, 6 months, 12 months
Radiologic outcome - time to union (fracture healing)	Radiologic outcome will be evaluated based on bridging callus evident on 2 x-ray views (AP and lateral). Time to union will be defined as bridging callus evide on 2 x-ray views.	baseline, 2 weeks, 6 weeks, 12 weeks, 6 months, 12 months
SF-36	36-item, self-reported questionnaire is an outcome tool that examines patient-reported overall health and ease of activities of daily living	baseline, 2 weeks, 6 weeks, 12 weeks, 6 months, 12 months
Pain Visual Analogue Score	• A standardized pain visual analogue scale will be used to rate pain with various activities of daily living on a scale from 0-10	baseline, 2 weeks, 6 weeks, 12 weeks, 6 months, 12 months
DASH score	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	baseline, 2 weeks, 6 weeks, 12 weeks, 6 months, 12 months

Collaborators and Investigators

• Sponsor: University of Calgary
• Collaborators: Canadian Orthopaedic Trauma Society; Canadian Orthopaedic Research Legacy; Calgary Surgical Research Development Fund; AO Research Fund
• Investigators: Principal Investigator: Paul J Duffy, MD, University of Calgary

Study record dates

Study Major Dates

• Study Start (Actual): July 2, 2010
• Primary Completion (Anticipated): March 8, 2023
• Study Completion (Anticipated): July 1, 2023

Study Registration Dates

• First Submitted: May 10, 2010
• First Submitted That Met QC Criteria: May 12, 2010
• First Posted (Estimate): May 14, 2010

Study Record Updates

• Last Update Posted (Actual): August 15, 2022
• Last Update Submitted That Met QC Criteria: August 10, 2022
• Last Verified: August 1, 2022

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Wounds and Injuries; Arm Injuries; Forearm Injuries; Fractures, Bone; Ulna Fractures
• Other Study ID Numbers: REB14-2004