Clinical Trials Directory

Trials / Terminated

TerminatedNCT01826942

Scar Prevention Using Fractional Carbon Dioxide Laser Treatment

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Lumenis Be Ltd. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

In this study the investigators intend to determine the impact of fractional CO2 laser treatment on the edges of a fresh wound during surgical area closure on thin skin (e.g. face, hands, arms, thorax, etc.) and on thick skin (abdominoplasty procedure) on scar formation. The investigators will also evaluate the effect of shallow fractional laser treatment versus deep parameters settings. If effective treatments could be performed at time of surgery, this would result in both time and cost saving to the patient and to the healthcare system and will improve patient's self-image post surgeries.

Conditions

Interventions

TypeNameDescription
DEVICELumenis UltraPulse single fractional CO2 laser treatment thin skin
DEVICESingle fractional CO2 treatment at surgical area closure procedure on thick skin

Timeline

Start date
2013-01-01
Primary completion
2013-03-01
Completion
2013-03-01
First posted
2013-04-09
Last updated
2014-03-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01826942. Inclusion in this directory is not an endorsement.

Scar Prevention Using Fractional Carbon Dioxide Laser Treatment (NCT01826942) · Clinical Trials Directory