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UnknownNCT03782038

Study to Evaluate the Efficacy of a Micro Coring Device for the Treatment of Scars of the Cytrellis Micro-Coring Device for the Treatment of Scars

A Prospective, Multi-center, Pilot Study to Evaluate the Safety and Efficacy of the Cytrellis Micro-Coring Device for the Treatment of Scars

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Cytrellis Biosystems, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

A study to evaluate the safety and effectiveness of a micro coring device for the treatment of scars.

Detailed description

The study subject population will consist to up to 30 subjects who meet the inclusion/exclusion criteria. All subjects will be monitored for a period of 6 months post last treatment. An study results will be assessed on the following: * POSAS - Patient Observer Scar Assessment * ASAS - Acne Scar Severity Scale * Subject Satisfaction Scale

Conditions

Interventions

TypeNameDescription
DEVICEMCDMicro coring skin removal with automated coring device

Timeline

Start date
2018-09-13
Primary completion
2019-09-17
Completion
2019-11-21
First posted
2018-12-20
Last updated
2018-12-21

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03782038. Inclusion in this directory is not an endorsement.

Study to Evaluate the Efficacy of a Micro Coring Device for the Treatment of Scars of the Cytrellis Micro-Coring Device (NCT03782038) · Clinical Trials Directory