Skin Elasticity Measurements in Face and Surgical Scars Across Age and Skin Types
This study aims to observe and compare the skin elasticity in scars and various facial and body parts among participants of different ages and skin types.
Data Collection
Collected from past medical records and data - RetrospectiveFibrosis+1
+ Pathologic Processes
+ Pathological Conditions, Signs and Symptoms
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: July 1, 2011
Actual date on which the first participant was enrolled.This study focuses on measuring skin elasticity, specifically on the face and surgical scars. It aims to compare changes in skin elasticity over a 3-month period between individuals who have undergone a skin resurfacing or tightening procedure and those who have not. The study also seeks to establish baseline elasticity scores for different age groups and skin types, as categorized by the Fitzpatrick scale. By doing so, the study hopes to provide valuable insights into how skin elasticity varies with age and skin type, potentially improving understanding and treatment of skin conditions. In this observational study, participants' skin elasticity will be measured at various body sites, including scarred sites, forehead, cheeks, mandible, and inner arm. The primary outcome is to compare the difference in skin elasticity measurements between participants of varying ages at these different anatomical sites. This comparison will help understand how skin elasticity changes with age and at different body locations.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.35 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Study Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Northwestern University Feinberg School of Medicine, Department of Dermatology
Chicago, United StatesOpen Northwestern University Feinberg School of Medicine, Department of Dermatology in Google Maps