A Retrospective Evaluation of Superficial Radiation Therapy (SRT) and Keloid Scars.
NCT ID: NCT03693924
Last Updated: 2018-10-03
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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UNKNOWN
100 participants
OBSERVATIONAL
2018-11-15
2019-02-16
Brief Summary
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Detailed Description
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About 18 million people worldwide are genetically prone to form keloids in response to skin trauma, with equal gender distribution and greater susceptibility for darker-skinned individuals and those aged 10 to 30 years.
The greatest obstacle in treating keloids with many available surgical and non-surgical methods is that new keloids typically recur at the site of excision due to the treatment itself. For example, the recurrence rate using surgical excision alone is 45 to 100 percent.
Surgical excision followed by radiotherapy is a helpful treatment option for large and more difficult-to-treat keloids that cannot otherwise be treated by, or have failed, more conservative measures. It is thought that because keloid fibroblasts are sensitive to x-ray irradiation, it may prevent the recurrence of keloids by controlling fibroblast proliferation, arresting the cell cycle, and inducing premature cellular senescence. When surgical keloid excision is followed by Radiation Therapy, recurrence drops dramatically to 10% or below.
The SRT-100™ is a United States Food and Drug Administration (U.S. FDA) approved device for delivering a precise, calibrated dose of Superficial Radiation Therapy (SRT) to treat keloids caused by surgery or injury. This retrospective study has been designed to focus on efficacy and safety of the SRT-100™ for the treatment of recurrent keloid scars.
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Interventions
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SRT-100
The SRT-100™ is a simple painless non-invasive in-office procedure that is approved by the U.S. Food and Drug Administration (U.S. FDA) to treat keloids caused by surgery or injury by delivering a precise, calibrated dose of Superficial Radiation Therapy (SRT) that only goes skin deep.
Eligibility Criteria
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Inclusion Criteria
* Treatment with SRT-100™ of one or more keloids.
* At least 1 year since treatment end.
* Required retrospective data is existing and sufficient.
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Sensus Healthcare
INDUSTRY
Responsible Party
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Principal Investigators
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Brian Berman, M.D.
Role: PRINCIPAL_INVESTIGATOR
Central Contacts
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Other Identifiers
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SRTS-SRT-002
Identifier Type: -
Identifier Source: org_study_id
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