- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00544635
The Effect Of Light On Scar Appearance
July 25, 2014 updated by: Northwestern University
The goal of this project is to examine the ability of light exposure to improve the appearance of cutaneous scars.
Study Overview
Status
Terminated
Conditions
Intervention / Treatment
Detailed Description
Light would be efficacious in improving scar appearance due to its known effects on wound healing, acne, and its use for skin rejuvenation.
Light interacts with cells and stimulates the production of new collagen and elastin.
This same energy can be used to inhibit collagen formation and help improve scars.
Study Type
Interventional
Enrollment (Anticipated)
50
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Illinois
-
Chicago, Illinois, United States, 60611
- Northwestern Memorial Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Have two lesions that have been selected for excision
- Have two cutaneous scars from previous excisions as part of a standard of care
- Subjects are in good health
- Subject has a willingness and the ability to understand and provide informed consent for the use of their tissue and communicate with the investigator
Exclusion Criteria:
- Pregnancy or lactation
- Subjects who are unable to understand the protocol or to give informed consent
- Subjects with mental illness
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: A
scars will be treated with light
|
scars will be treated with light
|
Placebo Comparator: B
no intervention
|
no intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Scar vascularity
Time Frame: 24 weeks
|
24 weeks
|
Scar pigmentation
Time Frame: 24 weeks
|
24 weeks
|
Scar thickness
Time Frame: 24 weeks
|
24 weeks
|
Scar length
Time Frame: 24 weeks
|
24 weeks
|
Scar width
Time Frame: 24 weeks
|
24 weeks
|
Scar surface area
Time Frame: 24 weeks
|
24 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2005
Primary Completion (Actual)
August 1, 2006
Study Completion (Actual)
August 1, 2006
Study Registration Dates
First Submitted
October 12, 2007
First Submitted That Met QC Criteria
October 12, 2007
First Posted (Estimate)
October 16, 2007
Study Record Updates
Last Update Posted (Estimate)
July 29, 2014
Last Update Submitted That Met QC Criteria
July 25, 2014
Last Verified
July 1, 2014
More Information
Terms related to this study
Other Study ID Numbers
- 1253-010
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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