A Trial Comparing Circumferential Casting Versus Splinting in Displaced Colles' Fractures
Primary Purpose
Colles' Fracture
Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Cylindrical cast
Modified sugar tong cast
Volar dorsal splint
Sponsored by
About this trial
This is an interventional treatment trial for Colles' Fracture focused on measuring Colles fracture treatment, Displaced fracture of distal radius, distal radius fracture treatment, RCT, Emergency Department, cast, splint, treatment
Eligibility Criteria
Inclusion Criteria:
- Age > 18 years
- Displaced fracture of distal radius requiring closed reduction
Exclusion Criteria:
- Open fracture
- Previous displaced fracture involving the same or contralateral distal radius
- neuromuscular deficits or CVA of either upper extremity that impaired functional outcome assessment
- concurrent carpal bone fractures or dislocations - - unstable fractures requiring primary open reduction and internal fixation
- skin allergy or sensitivity to either of the immobilization materials
- Smith's, Barton's or Chauffeur fractures
- Neurovascular compromise of the affected limb - - Bilateral distal radius fractures that prevented follow-up comparison with a normal contralateral limb
- Other significant and concurrent injuries in the ipsilateral extremity.
- Undisplaced distal radius fracture
- Reduction performed in the ED did not meet criteria for successful fracture reduction
Sites / Locations
- Department of Emergency Medicine, St Paul's Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
1
2
3
Arm Description
Cylindrical cast
Modified sugar tong cast
Volar dorsal splint
Outcomes
Primary Outcome Measures
Radiologic slippage of fracture at 4 weeks post reduction
Secondary Outcome Measures
Functional outcomes: DASH score, return to work, activities of daily living (ADL), wrist pain, range of motion (ROM) and grip strength
Full Information
NCT ID
NCT00704743
First Posted
June 23, 2008
Last Updated
June 24, 2008
Sponsor
University of British Columbia
Collaborators
Smith & Nephew, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT00704743
Brief Title
A Trial Comparing Circumferential Casting Versus Splinting in Displaced Colles' Fractures
Official Title
A Prospective Randomized Controlled Trial Comparing Circumferential Casting Versus Splinting in Displaced Colles' Fractures
Study Type
Interventional
2. Study Status
Record Verification Date
June 2008
Overall Recruitment Status
Completed
Study Start Date
November 1998 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
January 2004 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
University of British Columbia
Collaborators
Smith & Nephew, Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Displaced fractures of the distal radius requiring closed reduction (otherwise known as Colles fractures) are common in the emergency department. The purpose of the study is to determine if there is any difference between 3 methods of immobilization for these fractures: circumferential cast, volar-dorsal splint, and modified sugar tong splint. Maintenance of position was assessed at 4 weeks after the injury and wrist strength and function were assessed at 2 months and 6 months. We hypothesize that there will not be a clinically important difference between these methods of immobilizing for displaced fractures of the distal radius requiring closed reduction.
Extended description of the protocol, including information not already contained in other fields.
Objectives:
Primary: To determine the effectiveness of three immobilization methods (circumferential cast [CC], volar dorsal splint [VDS], modified sugar-tong [MST] splint) in maintaining the position of displaced distal radius fractures after successful closed reduction.
Secondary to assess long term functional outcomes associated with fiberglass splint immobilization versus standard cylindrical casting in patients maintaining initial non-operative reductions.
Design: Randomized prospective single blind controlled trial Patients/Participants: Patients over 18 years of age who presented to the emergency department with a displaced fracture of the distal radius, requiring closed reduction.
Outcome Measurements: Loss of reduction (radiological slippage or the need for surgical fixation during the 3-4 week primary immobilization period after initial successful reduction). Secondary outcomes were DASH score, return to work, activities of daily living (ADL), wrist pain, range of motion (ROM) and grip strength.
Study Phase Phase 3 Study Type Interventional - Assigned to treatment Recruitment status Completed 2003 Record Verification Date March 2003 Anticipated trial start date November 1998 Last Follow-Up Date December 2002 Data Entry Closure Date January 2004 Study Completion Date July 2004 Purpose Treatment Allocation Randomized
Masking Single Blind Control Active Assignment Parallel Endpoints Efficacy Primary outcome Radiologic slippage of fracture at 4 weeks post reduction
Key secondary outcomes Functional outcomes: DASH score, return to work, activities of daily living (ADL), wrist pain, range of motion (ROM) and grip strength
Detailed Description
Primary: To determine the effectiveness of three immobilization methods (circumferential cast [CC], volar dorsal splint [VDS], modified sugar-tong [MST] splint) in maintaining the position of displaced distal radius fractures after successful closed reduction.
Secondary to assess long term functional outcomes associated with fiberglass splint immobilization versus standard cylindrical casting in patients maintaining initial non-operative reductions.
Design: Randomized prospective single blind controlled trial Patients/Participants: Patients over 18 years of age who presented to the emergency department with a displaced fracture of the distal radius, requiring closed reduction.
Outcome Measurements: Loss of reduction (radiological slippage or the need for surgical fixation during the 3-4 week primary immobilization period after initial successful reduction). Secondary outcomes were DASH score, return to work, activities of daily living (ADL), wrist pain, range of motion (ROM) and grip strength.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colles' Fracture
Keywords
Colles fracture treatment, Displaced fracture of distal radius, distal radius fracture treatment, RCT, Emergency Department, cast, splint, treatment
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
120 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
Cylindrical cast
Arm Title
2
Arm Type
Active Comparator
Arm Description
Modified sugar tong cast
Arm Title
3
Arm Type
Active Comparator
Arm Description
Volar dorsal splint
Intervention Type
Device
Intervention Name(s)
Cylindrical cast
Intervention Description
Arm cast/immobilization technique for wrist fracture
Intervention Type
Device
Intervention Name(s)
Modified sugar tong cast
Intervention Description
Arm cast/immobilization technique for wrist fracture
Intervention Type
Device
Intervention Name(s)
Volar dorsal splint
Intervention Description
Arm cast/immobilization technique for wrist fracture
Primary Outcome Measure Information:
Title
Radiologic slippage of fracture at 4 weeks post reduction
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Functional outcomes: DASH score, return to work, activities of daily living (ADL), wrist pain, range of motion (ROM) and grip strength
Time Frame
4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age > 18 years
Displaced fracture of distal radius requiring closed reduction
Exclusion Criteria:
Open fracture
Previous displaced fracture involving the same or contralateral distal radius
neuromuscular deficits or CVA of either upper extremity that impaired functional outcome assessment
concurrent carpal bone fractures or dislocations - - unstable fractures requiring primary open reduction and internal fixation
skin allergy or sensitivity to either of the immobilization materials
Smith's, Barton's or Chauffeur fractures
Neurovascular compromise of the affected limb - - Bilateral distal radius fractures that prevented follow-up comparison with a normal contralateral limb
Other significant and concurrent injuries in the ipsilateral extremity.
Undisplaced distal radius fracture
Reduction performed in the ED did not meet criteria for successful fracture reduction
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Stenstrom, MD, Ph.D
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Eric Grafstein, MD
Organizational Affiliation
University of British Columbia
Official's Role
Study Director
Facility Information:
Facility Name
Department of Emergency Medicine, St Paul's Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V1Y 1Z1
Country
Canada
12. IPD Sharing Statement
Learn more about this trial
A Trial Comparing Circumferential Casting Versus Splinting in Displaced Colles' Fractures
We'll reach out to this number within 24 hrs