Post-Market Clinical Follow Up Study to Collect Additional Data and Imaging

Cynosure

Status: Completed

Conditions: Connective Tissue Defect

Treatments: Device: Shockwave Treatment

Study type: Interventional

Funder types: Industry

Identifiers

NCT04880070

SW-MCPM-2021

Details and patient eligibility

About

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.

Full 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.

Enrollment: 5 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• A healthy male or female 18 - 65 years of age.
• Willing to undergo treatments with the SoftWave device.
• Understands and accepts obligation not to receive any other procedures on the treatment area through the length of the study.
• Understands and accepts the obligation and is logistically able to be present for all visits.
• Is willing to comply with all requirements of the study and sign the informed consent document.

Exclusion criteria

• Is pregnant or of childbearing potential and not using medically effective birth control, or has been pregnant in the last 3 months, currently breast feeding or planning a pregnancy during the study.
• The subject has a pacemaker or implantable defibrillator.
• The subject has a severe coagulation disorder.
• The subject has open epiphyseal plates.
• The subject has recently had a steroid injection.
• The subject is currently enrolled in an investigational drug or device trial, or has received an investigational drug or been treated with an investigational device within in the area to be treated 6 months to entering this study.
• The subject has any condition or is in a situation which, in the Investigator's opinion, may put the subject at significant risk, may

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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5 participants in 1 patient group

Shockwave Device

Experimental group

Description:

The Shockwave device will be used on multiple areas of the body for the purpose of treating connective tissue.

Treatment:

Device: Shockwave Treatment