Clinical Trials Directory

Trials / Completed

CompletedNCT02032641

Evaluation of Non-Ablative Laser for Treatment of Direct Brow Lift Scars

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
9 (actual)
Sponsor
University of Miami · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine the efficacy of the 1064nm Neodymium yttrium aluminum garnet (Nd:YAG) laser (Laser Genesis, Cutera TM) in the treatment of surgical scar after direct brow lift.

Detailed description

Patients who undergo a direct brow lift may participate in this study. Participants will receive laser treatment on one of the two surgical wounds (side of treatment will be chosen randomly by an independent source). Treatment parameters will be 500 spots and 10-14 megajoules (mJ) depending on skin type. The opposite side brow scar will not be treated until 1 month after the study is completed (if the patient elects to treat the contralateral brow after study completion this will be done at no charge to the patient). This treatment will be given at 2-4 week intervals for 6 treatments. Photographs will be taken at each visit, and they will be assessed based on different parameters by an examiner, as well as judged by the patient based on overall appearance.

Conditions

Interventions

TypeNameDescription
DEVICELaser treatmentNon-ablative, non-fractional, microsecond-pulsed Nd:YAG laser 500-1000 pulses, 0.3 msec pulse duration, 10-14 J/cm2, 5 mm spot size

Timeline

Start date
2013-06-01
Primary completion
2015-05-01
Completion
2015-05-01
First posted
2014-01-10
Last updated
2017-01-27
Results posted
2017-01-27

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02032641. Inclusion in this directory is not an endorsement.