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NCT02466308 · ClinicalTrials.gov registry record · NA
Long Duration Therapeutic Ultrasound for Tendon Healing
A NA study of Tendinopathy and Tendinosis, sponsored by ZetrOZ.
- Completed
- Registry status
- NA
- Development phase
- 28
- Enrollment target
- 1
- Study location
NCT02466308 is a NA study of Tendinopathy and Tendinosis that has completed, run by ZetrOZ. The registered enrollment target is 28 participants, below the 1,064-participant average among 10 other Tendinopathy trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02466308, a NA study of Tendinopathy and Tendinosis, has completed, sponsored by ZetrOZ.
- COMPLETED
- Registry status
- NA
- Development phase
- 28 participants
- Enrollment target
- 1
- Study location
Study Summary
ZetrOZ's Ultrasonic Diathermy device (sam(R) Professional System) is intended for use as a portable and wearable medical device which, when applied to various areas of the body applies Low Intensity Therapeutic Ultrasound (LITUS) to deep tissues. This device is FDA-cleared for pain reduction, treatment of muscle spasm and joint contracture, and increasing local circulation. This study will look at the use of therapeutic ultrasound to relieve pain and enhance tendon extensibility for individuals with tendinopathy over a 6 week time period.
Conditions Studied
Interventions
- DEVICE SAM Ultrasound Diathermy Device
Study Locations (1)
Connecticut
- ZetrOZ, Inc. - Trumbull
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 28 participants |
| Start Date | 2014-02 |
| Est. Completion | 2014-09 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02466308
The ClinicalTrials.gov registry entry for NCT02466308 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 28 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,064-participant average among 10 other Tendinopathy trials with a reported enrollment target (97% lower). The listed sponsor is ZetrOZ, which has 17 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Tendinopathy appearing as the primary indexed condition, and to 1 intervention - of which SAM Ultrasound Diathermy Device is the first listed.
NCT02466308 reports 1 study location spanning 1 distinct geographic area - top geographies include Connecticut.
Frequently Asked Questions
What is clinical trial NCT02466308 about?
NCT02466308 is a clinical study titled "Long Duration Therapeutic Ultrasound for Tendon Healing". ZetrOZ's Ultrasonic Diathermy device (sam(R) Professional System) is intended for use as a portable and wearable medical device which, when applied to various areas of the body applies Low Intensity Therapeutic Ultrasound (LITUS) to deep tissues. This device is FDA-cleared for pain reduction, treatm...
What is the current status of trial NCT02466308?
This trial is currently completed. It is a NA study. The enrollment target is 28 participants. The study started on 2014-02. Estimated completion is 2014-09.
What conditions does trial NCT02466308 study?
This clinical trial studies the following conditions: Tendinopathy, Tendinosis, Tendinitis.
What interventions are being tested in trial NCT02466308?
The interventions under investigation include: SAM Ultrasound Diathermy Device (DEVICE).
Who is sponsoring clinical trial NCT02466308?
This trial is sponsored by ZetrOZ, which has 17 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02466308 being conducted?
This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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