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Skin Laxity clinical trials

View clinical trials related to Skin Laxity.

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NCT ID: NCT02444169 Completed - Skin Laxity Clinical Trials

Retrospective Evaluation of Combination Treatment With the Ulthera System

Start date: April 2015
Phase: N/A
Study type: Observational

A retrospective study to evaluate the Ulthera® System for its potential interaction with toxins and fillers. Up to 500 subjects will be enrolled.

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: 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: 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.

NCT ID: NCT01708512 Completed - Skin Laxity Clinical Trials

Feasibility Study: Higher Density Ulthera® System Treatment With Vectoring for Treatment of the Face and Neck

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

All enrolled subject will receive one Ultherapy™ treatment. Study images will be obtained pre-treatment, immediate post-treatment, and at each study follow-up visit. Enrolled subjects will return for follow-up visits at 90 days, 180 days and 365 days post-treatment.

NCT ID: NCT01708499 Completed - Skin Laxity Clinical Trials

Feasibility Study: Evaluation of the Ulthera® System for Treatment of Abdominal Tissue

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

Enrolled subjects will receive one UltherapyTM treatment on the abdomen. 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: NCT01708473 Completed - Skin Laxity Clinical Trials

Feasibility Study: Compare the Effectiveness Between Two Pain Medications When Used Prior to Ultherapy™ Treatments

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

This study will compare the effectiveness of two pain medications for reducing discomfort during an Ultherapy treatment.