N/A
N=100
Compass Hinge Stabilization of Knee Dislocations: A Randomized Trial
Knee Dislocation
Bottom Line
View on ClinicalTrials.gov: NCT00582517 ↗Enrolled (actual)
100
Serious AEs
0.0%
Results posted
Nov 2013
Primary outcome: Primary: Knee Stability — 29; 26; 12; 17 participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Compass Universal Hinge External Fixator (Device); Non-invasive External Knee Brace (Procedure)
- Age
- Adult, Older Adult · 19+ yrs
- Sex
- All
- Sponsor
- University of Alabama at Birmingham
- Primary completion
- Dec 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Knee Stability |
29; 26; 12; 17; 27; 30 | — |
Summary
The purpose of this project is to evaluate the effect of the Compass™ Universal Hinge external fixator on the outcome of patients following acute dislocation of the knee
Eligibility Criteria
Inclusion Criteria
- Trauma patient with a knee dislocation that requires surgical repair
- Adult patient (19 years and older)
Exclusion Criteria
- Patients unable or unwilling to comply with follow-up gait, radiographic and clinical evaluations necessary to complete the study
- Patients unable or unwilling to give informed consent and/or who have no responsible family member willing to give consent
- Pregnant women
- Prisoners
Data sourced from ClinicalTrials.gov (NCT00582517). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.