Application of the Apsara Thermal Wand System

Completed · Early Phase 1

Conditions studied: Tightening of Skin Laxity

In brief

The purpose of this feasibility study is to gain an initial assessment of the acute safety and performance of the Apsara Thermal Wand System in human facial tissue.

Key facts

Study ID

NCT00662389

Run by

Apsara Medical Corporation

People needed

4

Starts

2008-04-01

Expected to finish

2009-03-01

Last updated by the study team

2009-08-28

Who can join

Age: 40 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Nonsmoker
• Glogau class 1-3
• Previously chosen to undergo facelift

You may not qualify if…

• Pregnant, nursing
• Implanted electro-mechanical device
• Allergy to anesthesia or device metals
• Collagen vascular disease
• History of keloid or hypertrophic scar formation
• Uncontrolled diabetes
• Long term steroid or other immunologic inhibitor use
• Previous treatment to target area
• Does not consent to study
• Does not consent to photography or histological evaluation

Where it is running

• Bryant A. Toth, MD, FACS — San Francisco, California, United States

Full record on ClinicalTrials.gov

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