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Clinical Trials/NCT01688063
NCT01688063
Active, not recruiting
Not Applicable

A Pilot Study of Skin Elasticity Measurements of the Face and Surgical Scars Stratified by Age and Skin Type

Northwestern University1 site in 1 country35 target enrollmentJuly 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Skin Scarring
Sponsor
Northwestern University
Enrollment
35
Locations
1
Primary Endpoint
Skin elasticity measurement of participant's scars
Status
Active, not recruiting
Last Updated
last year

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
July 2011
End Date
December 2025
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Murad Alam

Professor in Dermatology, Otolaryngology - Head and Neck Surgery, and Surgery-Organ Transplantation

Northwestern University

Eligibility Criteria

Inclusion Criteria

  • Subject is 18-65 years of age
  • Subject scheduled to have resurfacing or tightening procedure done as Standard of Care (Arm 1, 25 subjects).
  • The subject has the willingness and the ability to understand and provide informed consent for the use of their tissue and communicate with the investigator
  • Subject is 18 and over
  • Subject has a linear surgical scar that is \> 2cm.
  • The subject has the willingness and the ability to understand and provide informed consent for the use of their tissue and communicate with the investigator

Exclusion Criteria

  • Part A, Group 1:
  • Subject is planning on having a cosmetic procedure done to their face during the 3 months they are participating in the study (Arm 2, 25 subjects).
  • Parts A and B:
  • Under 18 years of age
  • Pregnancy or Lactation
  • Subjects who are unable to understand the protocol or to give informed consent
  • Subjects with mental illness

Outcomes

Primary Outcomes

Skin elasticity measurement of participant's scars

Time Frame: up to 3 months

Difference in skin elasticity measurements will be compared between subjects of varying ages at different anatomical sites: scarred sites, forehead, cheeks, mandible, and inner arm.

Study Sites (1)

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