Finding studies
Finding studies
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Lead
Syneron Medical
This study is a Prospective clinical study to evaluate the Profound device for submental laxity. Up to a total of 60 healthy candidates, seeking treatment for submental laxity. Subjects will receive one Profound treatment targeted to both dermal and subcutaneous layer of the skin. Before treatment (15-20 minutes) the tissue to be treated will be injected with tumescence solution. Each subject will be followed for additional four (4) post treatment visits
Age
18–70
Sex
ALL
Healthy volunteers
Accepted
