Quantitative Evaluation of Skin Shrinkage Caused by a Non-invasive Tightening Device
NCT ID: NCT00894244
Last Updated: 2021-12-28
Study Results
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
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COMPLETED
NA
25 participants
INTERVENTIONAL
2009-04-30
2009-09-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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NA
SINGLE_GROUP
TREATMENT
SINGLE
Study Groups
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Treatment
Treatment using a non-invasive skin tightening radiofrequency device to observe skin shrinkage in the arms
Radiofrequency device
One treatment pass on one arm. 2-5 treatment passes on the other
Interventions
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Radiofrequency device
One treatment pass on one arm. 2-5 treatment passes on the other
Eligibility Criteria
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Inclusion Criteria
* Mild to moderate laxity of arm skin
* Skin of Fitzpatrick levels I-III
Exclusion Criteria
* Scarring or abnormalities in upper arm area
* Major systemic illnesses
* Any condition with delayed wound healing
* History of psychiatrist illnesses
30 Years
60 Years
ALL
Yes
Sponsors
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Northwestern University
OTHER
Responsible Party
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Murad Alam
Professor in Dermatology, Otolaryngology - Head and Neck Surgery, and Surgery-Organ Transplantation
Locations
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Northwestern University Feinberg School of Medicine, Department of Dermatology
Chicago, Illinois, United States
Countries
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Other Identifiers
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STU1178
Identifier Type: -
Identifier Source: org_study_id