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Wearable Therapeutic Ultrasound Study for Knee Osteoarthritis

NCT01993693 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2015-11-18

No results posted yet for this study

Summary

The purpose of this study is to evaluate the ability of a wearable therapeutic ultrasound device to reduce pain and increase mobility for subjects with knee osteoarthritis.

Conditions

Interventions

DEVICE

Ultrasonic Diathermy Device

The Ultrasonic Diathermy Device provides low intensity therapeutic ultrasound to musculoskeletal tissues and joints for the purpose of pain relief, relief of muscle spasm, treatment of joint contraction, and local increase of circulation. The device is FDA-cleared for up to 4 hours of continuous use per treatment. It is a stationary hands-free device.

DEVICE

Sham Ultrasonic Diathermy Device

Sham therapy delivered by Ultrasonic Diathermy Device that appears identical to active device but does not deliver ultrasound

Sponsors & Collaborators

  • State University of New York - Upstate Medical University

    collaborator OTHER

  • ZetrOZ, Inc.

    lead INDUSTRY

Principal Investigators

  • Timothy A. Damron, MD · SUNY Upstate Orthopedics

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
35 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-10-31
Primary Completion
2014-07-31
Completion
2014-07-31

Countries

  • United States

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 NCT01993693 on ClinicalTrials.gov