N/A
Completed N=100
Compass Hinge Stabilization of Knee Dislocations: A Randomized Trial
Knee Dislocation
Source: ClinicalTrials.gov NCT00582517 ↗
Enrolled (actual)
100
Serious AEs
0.0%
Results posted
Nov 2013
Primary outcomePrimary: Knee Stability — 29; 26; 12; 17 participants
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
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Knee Stability |
29; 26; 12; 17; 27; 30 | — |
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. Informational only — not medical advice.