CompletedNot Applicable

Quantitative Evaluation of Skin Shrinkage Caused by a Non-invasive Tightening Device

United States25 participantsStarted 2009-04

Plain-language summary

This study is being done to measure the amount of skin shrinkage caused by a non-invasive skin tightening device.

Who can participate

Age range30 Years – 60 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Age 30-60 y/o * Mild to moderate laxity of arm skin * Skin of Fitzpatrick levels I-III Exclusion Criteria: * Any active local arm infections * Scarring or abnormalities in upper arm area * Major systemic illnesses * Any condition with delayed wound healing * History of psychiatrist illnesses

What they're measuring

The Change in Skin Tightening in the Upper Inner or Outer Arm (as Measured by Millimeters)

Timeframe: immediately following treatment and 30 days after last treatment

Trial details

NCT IDNCT00894244

SponsorNorthwestern University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2009-09

Results submitted2012-02-07

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