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Clinical Trial Summary

The primary objective of Part A is to compare the change in elasticity measurements at baseline and at 3 months between subjects who have had a resurfacing or tightening procedure and those who have not. The secondary objective for Part A is to develop baseline elasticity scores for ages 18-35, 36-50, and 51-65 and for Fitzpatrick skin types I-II, III-IV, and V-VI. The primary objective of Part B is to compare the age of the scar and surrounding tissue with the elasticity measurements.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01688063
Study type Observational
Source Northwestern University
Contact
Status Active, not recruiting
Phase
Start date July 2011
Completion date December 2024

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