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Use of Cold and Compression Therapy With Total Knee Replacement Patients

NCT00712816 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 224

Last updated 2012-03-20

No results posted yet for this study

Summary

The purpose of the study is to evaluate the effectiveness of a device that delivers cold and intermittent compression as compared to ice and compressive wraps on patients who have undergone knee replacement.

Conditions

Interventions

DEVICE

Game Ready Injury Treatment System (CoolSystems Inc.)

Cold with intermittent compression postoperatively for 2 weeks

OTHER

Ice with compressive bandages

Cold with static compression postoperatively for 2 weeks

Sponsors & Collaborators

  • CoolSystems, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-07-31
Primary Completion
2011-12-31
Completion
2012-05-31

Countries

  • United States
  • Australia

Study Locations

More Related Trials

Entities

Diseases

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 NCT00712816 on ClinicalTrials.gov