Post-Market Clinical Follow Up Study to Collect Additional Data and Imaging
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- STATUS
- Recruiting
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- days left to enroll
- 2
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- participants needed
- 50
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- sponsor
- Cynosure, Inc.
Summary
This is a prospective, open label, multi-center clinical study to collect additional data and imaging for the ViaSure device.The intended use of the ViaSure device used in this study is to assess the usability and tissue response to shock wave treatment.
Description
Up to 50 subjects will be enrolled at 2 study centers. Subjects will attend a screening/pretreatment visit which may be performed on the same day as the treatment visit. Subjects may receive up to 5 treatments with the study device. Follow up visits may occur 30 and 90 days post last treatment visit.
Details
| Condition | Connective Tissue Defect |
|---|---|
| Treatment | Shockwave Treatment |
| Clinical Study Identifier | NCT04880070 |
| Sponsor | Cynosure, Inc. |
| Last Modified on | 27 April 2022 |
How to participate?
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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