The Effect Of Light On Scar Appearance
This study has been terminated.
(Study personnel left institution before study completion.)
Sponsor:
Northwestern University
Information provided by:
Northwestern University
ClinicalTrials.gov Identifier:
NCT00544635
First received: October 12, 2007
Last updated: July 12, 2011
Last verified: July 2011
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Purpose
Detailed Description:
The goal of this project is to examine the ability of light exposure to improve the appearance of cutaneous scars.
Condition | Intervention |
---|---|
Cutaneous Scars |
Device: no intervention Device: light |
Study Type: | Interventional |
Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
Official Title: | The Effect Of Light On Scar Appearance |
Resource links provided by NLM:
Further study details as provided by Northwestern University:
Primary Outcome Measures:
- Scar vascularity [ Time Frame: 24 weeks ] [ Designated as safety issue: No ]
- Scar pigmentation [ Time Frame: 24 weeks ] [ Designated as safety issue: No ]
- Scar thickness [ Time Frame: 24 weeks ] [ Designated as safety issue: No ]
- Scar length [ Time Frame: 24 weeks ] [ Designated as safety issue: No ]
- Scar width [ Time Frame: 24 weeks ] [ Designated as safety issue: No ]
- Scar surface area [ Time Frame: 24 weeks ] [ Designated as safety issue: No ]
Estimated Enrollment: | 50 |
Study Start Date: | November 2005 |
Study Completion Date: | August 2006 |
Primary Completion Date: | August 2006 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
---|---|
Experimental: A
scars will be treated with light
|
Device: light
scars will be treated with light
|
Placebo Comparator: B
no intervention
|
Device: no intervention
no intervention
|
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.
Eligibility
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Criteria
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
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00544635
Locations
United States, Illinois | |
Northwestern Memorial Hospital | |
Chicago, Illinois, United States, 60611 |
Sponsors and Collaborators
Northwestern University
Investigators
Principal Investigator: | Murad Alam, MD | Northwestern University |
More Information
No publications provided
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on October 17, 2012
No publications provided
Responsible Party: | Murad Alam, MD, Northwestern University |
ClinicalTrials.gov Identifier: | NCT00544635 History of Changes |
Other Study ID Numbers: | 1253-010 |
Study First Received: | October 12, 2007 |
Last Updated: | July 12, 2011 |
Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
Cicatrix Fibrosis Pathologic Processes |
ClinicalTrials.gov processed this record on October 17, 2012