Wearable Therapeutic Ultrasound Study for Knee Osteoarthritis

Knee Osteoarthritis Clinical Trial

Official title:

Wearable Therapeutic Ultrasound Study

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01993693
• Other study ID #: OA-02
• Secondary ID: 2012-1
• Status: Terminated
• Phase: N/A
• First received: October 24, 2013
• Last updated: November 17, 2015
• Start date: October 2012
• Est. completion date: July 2014

Study information

• Verified date: June 2014
• Source: ZetrOZ, Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review BoardUnited States: Food and Drug Administration
• Study type: Interventional

Clinical Trial 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.

Description:

Up to 50 million people in the U.S. suffer from some form of chronic pain, and 60% of these Americans are under 65 and have limited mobility because of knee or hip Osteoarthritis (OA). Pharmaceuticals currently dominate the treatment options due to widespread insurance coverage and convenience. However, there are a myriad of public health problems associated with analgesic use, including costs, untoward side effects, and addiction potential with opioid analgesics.

Ultrasound therapy for pain and healing has been approved by the U.S. FDA and has been in use around the globe for the last 60 years. Traditionally, ultrasound-mediated pain treatment has been delivered in clinics and has been limited to short and confined periods of 5-15 min at acoustic intensities from 1-4 W/cm2 over a course of weeks to months. Over the past decade, research has increasingly focused on lower-intensity therapeutic ultrasound (30-1000 mW/cm2) delivered over extended 1-8 hr periods. (mW = milliwatt) Recent animal studies using low-intensity therapeutic ultrasound (LITUS) have demonstrated successful inflammation reduction, reduced cartilage degeneration, and tendon and fracture healing. It is believed that using a lower-intensity ultrasonic treatment regimen over extended treatment periods works with the body's natural healing process and minimizes acoustic insult as compared with traditional, higher intensity treatments. This study proposes to evaluate clinically the first wearable low intensity ultrasound system for noninvasive treatment of arthritis pain. This technology has the potential to measurably increase the quality of life for millions of people who suffer from osteoarthritis pain by providing a safe, effective, and easy-to-use treatment.

The pilot study will test the versatile ultrasound therapy system in a clinical study that will enroll up to 60 patients with mobility-impairing knee OA. The goal of the study is to establish statistically significant data that daily 4 hour LITUS treatment decreases participant pain (Visual Analog Scale [VAS]) and improves patient mobility (measured by an accelerometer worn by each participant) over placebo devices.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 15
• Est. completion date: July 2014
• Est. primary completion date: July 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 35 Years to 80 Years

Eligibility

Individual will be included if they:

1. Have physician-diagnosed mild to moderate knee OA (OARSI atlas grades 1-2) based on fixed-flexion x-ray radiological findings for osteophytes and joint space narrowing within the past 12 months,

2. are between 35-65 years of age

3. report a frequent pain score between 4-7 (range: 0-10) during the week preceding enrollment

4. report mobility limitations because of their knee pain

5. are currently not taking any prescription pain medication other than nonsteroidal antiinflammatory drugs (NSAIDs). All pain medication taken during the study should be documented.

6. are willing not to use any cream, gel, or topical solution during the administration of treatment other than the approved ultrasound gel provided to the subject at the initiation of the study

7. are deemed appropriate by their physician to participate.

Individuals will be excluded if they:

1. cannot successfully demonstrate the ability to put on and take off the device

2. are cognitively impaired

3. have bone-on-bone crepitus

4. have severe OA or patients with little to no cartilage on the knee

5. have knee replacement or other surgical intervention

6. take variable prescription medication

7. are non-ambulatory

8. participated in a clinical trial for an investigational drug and/or agent within 30 days prior to screening

9. are currently taking neuropathic medications (ie: Neurontin, Lyrica or Topamax) and/or antidepressants (ie: Amitriptyline).

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Knee Osteoarthritis
• Osteoarthritis
• Osteoarthritis, Knee

Intervention

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

Locations

Country	Name	City	State
United States	Upstate Orthopedics	East Syracuse	New York

Sponsors (2)

Lead Sponsor	Collaborator
ZetrOZ, Inc.	State University of New York - Upstate Medical University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain	Pain will be recorded using the Visual Analogue Scale (VAS).	Pain will be recorded twice a day, immediately before application of the device and then immediately after the 4 hour treatment.	No
Secondary	Mobility	Mobility will be measured using an actigraph that will be worn on the subject's wrist 24 hours a day.	Mobility will be recorded logged every 5 minutes, up to 24 hours a day, by the actigraph that the subject is wearing on their wrist.	No