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Efficacy and Safety of Rebel Reliever Brace in Patients With Symptomatic Medial Knee Osteoarthritis

NCT02021136 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 67

Last updated 2016-12-30

No results posted yet for this study

Summary

The purpose of the study is to evaluate the superiority of Rebel Reliever® knee brace + standard treatment versus standard treatment alone in terms of last 24-hour pain relief after 6 weeks. in patients with medial knee osteoarthritis.

Conditions

  • Osteoarthritis, Knee

Interventions

DEVICE

Rebel Reliever

Rebel Reliever knee brace + usual antalgic treatment + physical exercises recommendations

OTHER

Control

Usual antalgic treatment + physical exercises recommendations

Sponsors & Collaborators

  • Thuasne

    lead INDUSTRY

Principal Investigators

  • Philippe THOUMIE, MD · Coordinator

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-10-31
Primary Completion
2016-07-31
Completion
2016-09-30

Countries

  • France

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 NCT02021136 on ClinicalTrials.gov