Clinical Trials Directory

Trials / Completed

CompletedNCT02050126

Caesarean Scar Revision With the UltraPulse

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Lumenis Be Ltd. · Industry
Sex
Female
Age
22 Years – 55 Years
Healthy volunteers
Accepted

Summary

Ten (10) adult female subjects that had a caesarean surgery performed.Study will be conducted in 1 site. Each subject will receive three treatments on one area that was randomly chosen. The other area will be left untreated and will serve as a control. The objective is to Evaluate the clinical impact of UltraPulse fractional carbon dioxide laser treatment on the appearance of a Caesarean Scar (CS) as compared to a similar untreated scar side.

Conditions

Interventions

TypeNameDescription
DEVICELumenis UltraPulse Encore.Treatment using Lumenis UltraPulse Encore.

Timeline

Start date
2013-04-01
Primary completion
2016-01-01
Completion
2016-01-01
First posted
2014-01-30
Last updated
2016-04-22

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT02050126. Inclusion in this directory is not an endorsement.