N/A N=25 Single-blind Treatment

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

Healthy

Bottom Line

View on ClinicalTrials.gov: NCT00894244 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Sep 2012

Primary outcome: Primary: The Change in Skin Tightening in the Upper Inner or Outer Arm (as Measured by Millimeters) — 45.17 millimeters

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Radiofrequency device (Device)
Age: Adult · 30+ yrs
Sex: All
Sponsor: Northwestern University
Primary completion: Sep 2009

Outcome Measures

Outcome	Result	p-value
PRIMARY The Change in Skin Tightening in the Upper Inner or Outer Arm (as Measured by Millimeters)	45.17	—

Summary

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

Eligibility Criteria

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

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00894244). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.