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Treatment of Distal Radius Fractures in Elderly Patients

Treatment of Distal Radius Fractures in Elderly Patients, a Randomized Controlled Trial

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00788190
Enrollment
65
Registered
2008-11-10
Start date
2008-11-30
Completion date
Unknown
Last updated
2011-04-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Distal Radius Fractures

Keywords

Distal Radius Fracture, Elderly, Prospective randomized trial, Outcomes, Pain and Function, Surgical Vs. conservative management, Fractures with borderline alignment

Brief summary

The purpose of this study is to create and test a treatment algorithm to guide the treatment of distal radius fractures in patients 65 and older and to obtain level-one evidence to determine the best method of treating distal radius fractures in this growing population demographic.

Detailed description

* Distal radius fractures with borderline alignment will be randomized to surgical intervention or conservative treatment. * Patients will fill out subjective questionnaires at 0, 6weeks, 3months, 6 months, and 1 year. * Patients will perform objective strength tests, dexterity tests and have their range of motion tested at 12 weeks, 6 months and 12 months.

Interventions

PROCEDUREDistal Radius Fracture Reduction

Surgical Intervention to Reduce Distal Radius Fracture

Conservative management of Distal Radius Fractures

Sponsors

LHRI- Lawson Health Research Institute
CollaboratorUNKNOWN
Hand and Upper Limb Clinic, Canada
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Distal Radius Fracture * Between 10 and 20 degrees of dorsal angulation * Between 3 and 5mm of Ulnar positive variance * Between 1 and 2mm intra Articular Step deformity * Age 65 and older

Exclusion criteria

* Pre-Morbid medical conditions which preclude surgical intervention * Patients who do not live independently. * Patients with an open fracture * Associated soft tissue or skeletal injury to the same limb. * Pre-existing wrist arthrosis or disability

Design outcomes

Primary

MeasureTime frame
Primary: Patient pain and disability. Will be quantified with Disabilities of the Arm and Shoulder (DASH) and Patient Rated Wrist Evaluation (PRWE).0-1 year

Secondary

MeasureTime frame
Secondary: To determine if other baseline factors influence outcome. For example, baseline activity levels (RAPA), home supports, hand dominance, and general mental health will be analyzed.over 1 year
Secondary: To stratify results by age. (65-75, 77-80, and >80)0-1 year
Grip strength, Range of Motion and Dexterity testing of wrists3 months to 12 months

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026