A Prospective Study Comparing Different Clinical Decision Rules in Adult and Pediatric Ankle Trauma

NCT01205841 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1500

Last updated 2010-09-21

No results posted yet for this study

Summary

Comparison of the reliability of different examination techniques to detect fractures in patients with ankle trauma.

Conditions

  • Ankle Injuries

Interventions

PROCEDURE

Ottawa Ankle and Foot Rules

As previously published

PROCEDURE

Buffalo Rule

As previously published

PROCEDURE

Ottawa Ankle and Foot Rules + application of a tuning fork to the distal fibula and tibia

As previously published

PROCEDURE

Thompson Test

As previously published

PROCEDURE

Palpation of the fibula

Palpation of the fibula over its entire length.

PROCEDURE

Ottawa Ankle and Foot Rules + palpation of the cuboid bone

As previously published

PROCEDURE

Ottawa Ankle and Foot Rules + palpation over the deltoid ligament

As previously published

PROCEDURE

Malleolar Zone Algorithm

As previously published

PROCEDURE

Low Risk Exam

As previously published

PROCEDURE

Bernese Ankle Rules

As previously published

PROCEDURE

Ottawa Ankle and Foot Rules + swelling of the distal fibula

As previously published

Sponsors & Collaborators

  • KU Leuven

    lead OTHER

Principal Investigators

  • Dimitri Vandoninck, MD · Emergency Department of the University Hospitals, Catholic University Leuven

  • Marc Sabbe, MD, PhD · Emergency Department of the University Hospitals, Catholic University Leuven

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
5 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-09-30
Primary Completion
2012-08-31
Completion
2012-08-31

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01205841 on ClinicalTrials.gov