Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
50 participants
INTERVENTIONAL
2005-11-30
2006-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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A
scars will be treated with light
light
scars will be treated with light
B
no intervention
no intervention
no intervention
Interventions
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no intervention
no intervention
light
scars will be treated with light
Eligibility Criteria
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Inclusion Criteria
* 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
* Subjects who are unable to understand the protocol or to give informed consent
* Subjects with mental illness
18 Years
ALL
No
Sponsors
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Northwestern University
OTHER
Responsible Party
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Northwestern University
Principal Investigators
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Murad Alam, MD
Role: PRINCIPAL_INVESTIGATOR
Northwestern University
Locations
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Northwestern Memorial Hospital
Chicago, Illinois, United States
Countries
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Other Identifiers
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1253-010
Identifier Type: -
Identifier Source: org_study_id
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