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Skin Laxity clinical trials

View clinical trials related to Skin Laxity.

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NCT ID: NCT02441036 Terminated - Skin Laxity Clinical Trials

Gene Expression Following Ultherapy® Treatment

Start date: May 1, 2015
Phase: N/A
Study type: Interventional

Up to 25 subjects will be enrolled and randomized. Randomized subjects will receive one single-side Ulthera® treatment in the pre-auricular region on the face. At each subject's scheduled facelift procedure, resected tissue will be obtained for analysis.

NCT ID: NCT02416076 Completed - Skin Laxity Clinical Trials

Ultherapy® for Treating the Face and Neck Using Standard Versus Simulines Transducers

Start date: December 15, 2014
Phase: N/A
Study type: Interventional

Up to 40 participants will be enrolled, randomized and treated. Enrolled participants will receive one, split-face Ulthera® treatment on the face and neck using a Ulthera System standard transducer on one side of the face and a Ulthera System prototype simulines transducers on the other side of the face. Follow-up visits will occur at 90 and 180 days post-treatment. Study images will be obtained pre-treatment, immediately post-treatment, and at each follow-up visit.

NCT ID: NCT01971736 Completed - Skin Laxity Clinical Trials

Efficacy of Long Pulsed 1064nm Laser for Facial Skin Tightening

Start date: September 2012
Phase: N/A
Study type: Observational

We study the efficacy of 1 pass of stacking pulses of long pulse 1064nm laser on the face for skin tightening immediately post laser and 3 months follow up.

NCT ID: NCT01735929 Withdrawn - Skin Laxity Clinical Trials

Combination of Ultrasound Treatment and Neck Liposuction for Skin Tightening

Start date: March 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to find out the effectiveness of ultrasound treatment and liposuction combined on skin tightening around the neck.

NCT ID: NCT01713998 Completed - Skin Laxity Clinical Trials

Treatment of the Face and Neck With Lower Ulthera System Energy Settings

Start date: September 2011
Phase: N/A
Study type: Interventional

Up to 60 subjects will be enrolled. Enrolled subjects will receive one Ulthera® treatment on the face and neck. Follow-up visits will occur at 90 and 180 days post-treatment. Study images will be obtained pre-treatment, immediately post-treatment, and at each follow-up visit.

NCT ID: NCT01713985 Completed - Skin Laxity Clinical Trials

Feasibility Study: Evaluation of Ulthera Versus Thermage for Treating the Face and Neck

Start date: September 2012
Phase: N/A
Study type: Interventional

Up to 20 subjects will be enrolled and randomly assigned to one of two treatment groups. Group A will receive Ultherapy™ on the right side of the face and neck and Thermage on the left side. Group B will receive Thermage on the right side of the face and neck and Ultherapy™ on the left side. Follow-up visits will occur at 90 and 180 days post-treatment. Study images will be obtained pre-treatment, immediately post-treatment, and at each follow-up visit.

NCT ID: NCT01713907 Terminated - Skin Laxity Clinical Trials

Evaluation of the Ulthera® System for Treatment of the Face and Neck

Start date: June 2011
Phase: N/A
Study type: Interventional

Up to 15 subjects will be enrolled. Enrolled subjects will receive one Ulthera® treatment on the face and neck. Follow-up visits will occur at 45, 90 and 180 days post-treatment. Study images will be obtained pre-treatment, immediately post-treatment, and at each follow-up visit.

NCT ID: NCT01713569 Terminated - Skin Laxity Clinical Trials

Feasibility Study: Histological Characterization After Treatment With the Ulthera® System

Start date: October 2012
Phase: N/A
Study type: Interventional

Up to 6 subjects will be enrolled. Subjects who have already chosen to have a surgical facelift procedure will be enrolled. Subjects will receive selective Ulthera® ultrasound exposures in the pre-auricular regions. Subject will return for a follow-up visit up to 48 hours post-treatment, on the day of their rhytidectomy. Study images will be obtained pretreatment, immediately post-treatment, and at the follow-up visit.

NCT ID: NCT01708928 Completed - Skin Laxity Clinical Trials

Feasibility Study: Lifting and Tightening Neck Skin in Patients

Start date: August 2010
Phase: N/A
Study type: Interventional

Up to 30 subjects will be enrolled. All subjects will receive one Ultherapy treatment to the lower two thirds of the face and neck. Subjects will be equally grouped into those with a history of submentoplasty and or rhytidectomy and those naive to submentoplasty and or rhytidectomy. Follow-up visits will occur at 14, 30, 60, 90 and 180 days following treatment. Study images will be obtained pre-treatment, 30-60 minutes post-treatment, and at each follow-up visit.

NCT ID: NCT01708525 Completed - Skin Laxity Clinical Trials

Feasibility Study: Heavy Water Tissue Labeling Protocol

Start date: August 2012
Phase: N/A
Study type: Interventional

Enrolled subjects undergo tissue labeling to evaluate the rate of collagen synthesis in tissue treated with the Ulthera® System compared to control tissue.