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Trial registered on ANZCTR
Registration number
ACTRN12614000323628
Ethics application status
Approved
Date submitted
11/03/2014
Date registered
26/03/2014
Date last updated
26/03/2014
Type of registration
Retrospectively registered
Titles & IDs
Public title
Fractures of the distal radius: a randomized controlled trial of 180 patients comparing volar locking plates and traditional surgical treatment
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Scientific title
In treating patients with distal radius fractures, do volar locking plates produce better outcomes than traditional surgical treatment when assessed by DASH score primarily with function and radiological assessment as secondary outcomes.
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Secondary ID [1]
284237
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Nil
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Universal Trial Number (UTN)
U1111-1154-3526
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Fracture of the distal radius
291349
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Condition category
Condition code
Surgery
291712
291712
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0
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Surgical techniques
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Injuries and Accidents
291773
291773
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0
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Fractures
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Volar locking plate fixation of distal radius fracture. Surgery involves a volar approach to the distal radius and fixation with a plate which utilises locking screw heads. This is designed to provide a stable construct, supporting the chondral surface and allowing early mobilisation. Surgery takes about an hour.
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Intervention code [1]
288944
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Treatment: Surgery
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Intervention code [2]
288945
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Treatment: Devices
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Comparator / control treatment
Surgical treatment of distal radius fractures other than Volar Locking Plate, including Kirschner wires, non-locking plates and external fixateur. Choice of which surgical procedure in this group is at the discretion of the treating physician but excludes Volar Locking Plate.
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Control group
Active
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Outcomes
Primary outcome [1]
291654
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DASH score
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Assessment method [1]
291654
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Timepoint [1]
291654
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One week post surgery, 12 weeks, 52 weeks.
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Secondary outcome [1]
307238
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Range of motion of the affected wrist, both actual range and as a percentage of the unaffected wrist motion, measured with a goniometer placed at the axis of wrist motion and measured in three planes.
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Assessment method [1]
307238
0
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Timepoint [1]
307238
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One, 6, 12, 52 weeks after surgery
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Secondary outcome [2]
307239
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Grip strength measured with a Jamar Dynamometer and averaged over three readings, recorded in kilograms and expressed as a percentage of the uninjured side.
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Assessment method [2]
307239
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Timepoint [2]
307239
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One, 6, 12, 52 weeks post operation.
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Secondary outcome [3]
307240
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Radiological measurement, radial length, angle, inclination and step
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Assessment method [3]
307240
0
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Timepoint [3]
307240
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Initial, in theatre, one, 6, 12 weeks post operation.
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Eligibility
Key inclusion criteria
Patients with a distal radius fracture requiring surgical fixation, over 18 years old.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Cognitive incapacity, neurological disorders affecting coordination or function, pre-existing upper limb deformity or disability and concurrent upper limb injury.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Sealed opaque envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation from table
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
13/08/2005
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Actual
13/08/2005
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Date of last participant enrolment
Anticipated
24/04/2009
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Actual
24/04/2009
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
180
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
SA
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Recruitment hospital [1]
2181
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Flinders Medical Centre - Bedford Park
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Recruitment postcode(s) [1]
7859
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5042 - Bedford Park
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Funding & Sponsors
Funding source category [1]
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Self funded/Unfunded
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Name [1]
288865
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Peter Tamblyn
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Address [1]
288865
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Flinders Medical Centre,
Bedford Drive
Bedford Park,
South Australia 5042
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Country [1]
288865
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Australia
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Primary sponsor type
Hospital
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Name
Flinders Medical Centre
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Address
Bedford Drive
Bedford Park,,
South Australia 5042
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Country
Australia
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Secondary sponsor category [1]
287561
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None
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Name [1]
287561
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Address [1]
287561
0
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Country [1]
287561
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
290694
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Flinders Medical Centre Ethics Committee
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Ethics committee address [1]
290694
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Bedford Drive, Bedford Park, South Australia 5042
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Ethics committee country [1]
290694
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Australia
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Date submitted for ethics approval [1]
290694
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Approval date [1]
290694
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11/07/2005
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Ethics approval number [1]
290694
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Summary
Brief summary
Fractures of the distal radius,: a randomised controlled trial comparing the volar locking plate and routine current surgical treatment
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Trial website
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Trial related presentations / publications
Nil
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Public notes
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Contacts
Principal investigator
Name
46842
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Dr Peter Tamblyn
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Address
46842
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Department of Orthopaedic Surgery,
Bedford Drive,
Flinders Medical Centre,
Bedford Park,
South Australia 5042
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Country
46842
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Australia
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Phone
46842
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+618 82044289
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Fax
46842
0
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Email
46842
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[email protected]
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Contact person for public queries
Name
46843
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Peter Tamblyn
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Address
46843
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Department of Orthopaedic Surgery,
Bedford Drive,
Flinders Medical Centre,
Bedford Park,
South Australia 5042
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Country
46843
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Australia
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Phone
46843
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+618 82044289
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Fax
46843
0
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Email
46843
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[email protected]
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Contact person for scientific queries
Name
46844
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Peter Tamblyn
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Address
46844
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Department of Orthopaedic Surgery,
Bedford Drive,
Flinders Medical Centre,
Bedford Park,
South Australia 5042
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Country
46844
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Australia
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Phone
46844
0
+618 82044289
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Fax
46844
0
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Email
46844
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
Download to PDF