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Clinical Trial Summary

To evaluate the safety, and efficacy of the ASR device for the temporary improvement in the appearance of a keloids.


Clinical Trial Description

To evaluate the safety, and efficacy of the ASR device for the temporary improvement in the appearance of a keloids. To demonstrate improvement in the keloid scars, without unexpected adverse events (UAEs) and serious adverse events (SAEs) directly attributable to the ASR device or treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04016610
Study type Interventional
Source Soliton
Contact
Status Completed
Phase N/A
Start date July 9, 2019
Completion date February 12, 2020

See also
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Completed NCT04786210 - Treatment of Keloids With Fractional Erbium Laser-Assisted 5-Fluorouracil Versus Laser-Assisted Corticosteroid Phase 4
Not yet recruiting NCT02521402 - Pilot Study to Evaluate Clinical Outcomes With the Use of Biovance Following Keloid Scar Revision Surgery Phase 4
Active, not recruiting NCT01736969 - A Substantial Equivalence Study of RD04723 and Predicate Device N/A
Completed NCT01176877 - Assessing and Improving Patient Knowledge About Keloid Scars (Keloids) N/A
Recruiting NCT04184011 - Superficial Radiation Therapy (SRT) for the Treatment of Recurrent Keloid Scars
Withdrawn NCT01295099 - Keloid Scarring: Treatment and Pathophysiology Phase 4