Distal Radius Fracture Clinical Trial
Official title:
Outcome Assessment in the Treatment of Type A2 Fractures of the Distal Radius by Short Arm Cast Versus Long Arm Cast
Verified date | November 2014 |
Source | Mashhad University of Medical Sciences |
Contact | n/a |
Is FDA regulated | No |
Health authority | Iran: Ethics Committee |
Study type | Interventional |
Distal radius fracture (DRF) is among the most common fractures of the long bones, which comprise one sixth of all fractures. Due to its high prevalence, effect on patients' everyday life, and cost on national health resources, its proper management is very important. The investigators performed this prospective randomized clinical trial on 100 patients with DRFs. 50 patients were treated in each group either by short or long arm cast. Patients were visited during the 6th and 18th weeks after the reduction regarding loss of reduction and possible complications.
Status | Completed |
Enrollment | 100 |
Est. completion date | February 2011 |
Est. primary completion date | February 2011 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 20 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Older than 20 years - Type A2 according to the AO classification - Closed distal radial physis - Initial radiographic evidence of extra articular DRF - With at least one non-comminuted cortex Exclusion Criteria: - Fractures with dorsal angulations of more than 20 degrees - Radial shortening of more than 10 millimeters - Extensive cortical comminution as unstable fractures - Patients with unstable fractures - Existence of multiple fractures or open fracture in the affected limb or other limbs - Cerebral palsy - Paresthesia of the affected limb due to the pervious cerebro-vascular accidents - Previous severe deformity of the affected limb diabetes - Severe osteoporosis - Less than two consecutive follow-up visits |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Mashhad University of Medical Sciences |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Range of Motion | Elbow flexion-extension and forearm supination-pronation | 18 weeks after closed reduction | No |
Secondary | Number of Participants with Adverse Events as a Measure of Safety and Tolerability | Distal radioulnar joint instability | 18 weeks after closed reduction and casting | No |
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