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Skin Laxity clinical trials

View clinical trials related to Skin Laxity.

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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.

NCT ID: NCT01708460 Completed - Skin Laxity Clinical Trials

Feasibility Study: Ulthera Treatment of the Buttocks and Thighs

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

Up to 30 subjects will be enrolled. Enrolled subjects will receive an Ulthera® treatment to one side of the body, treating the lateral buttock region. 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: NCT01708447 Completed - Skin Laxity Clinical Trials

Feasibility Study: Evaluate the Effectiveness of Using a Topical Anesthetic Prior to Ultherapy™ Treatment

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

This study will evaluate the efficacy of a lidocaine topical anesthetic (numbing cream) for reducing discomfort associated with Ultherapy™ treatment.

NCT ID: NCT01708434 Completed - Skin Laxity Clinical Trials

Feasibility Study: Evaluation of the Ulthera® System for Treatment of the Knees

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

Enrolled subjects will receive one bilateral Ulthera® treatment on the knees. Up to 30 subjects will be enrolled. Study photos will be obtained prior to study treatment, immediately following study treatment, and at each post-treatment follow-up visit. Follow-up visits will occur at 90 and 180 days post-treatment.

NCT ID: NCT01708382 Completed - Skin Laxity Clinical Trials

Feasibility Study: Lifting and Tightening of the Elbows

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

Up to 20 subjects will be treated. Treated subjects will receive one Ulthera® treatment on the elbows. 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: NCT01708252 Completed - Skin Laxity Clinical Trials

Feasibility Study: Treatment of Post-surgery and Surgery Naive Patients Who Failed to Respond to a Previous Ulthera Treatment

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

Up to 10 subjects will be enrolled. All subjects will receive an increased density UltherapyTM treatment at dual depth. Treatments will be provided to the lower 2/3 of the face and neck. Follow-up visits will occur at 90 and 180 days post-treatment. Study images will be obtained pre-treatment, 30-60 min post-treatment, and at each follow-up visit.

NCT ID: NCT01519934 Completed - Skin Laxity Clinical Trials

A Retrospective Study to Evaluate the Effectiveness of the Ulthera System

Start date: October 2011
Phase: N/A
Study type: Observational

Up to 120 subjects within the study site's practice who have already had an Ultherapy™ treatment to the face and neck will be enrolled to monitor treatment effectiveness. Follow-up visits will occur at 90 and 180 days post-treatment. Study images will be obtained at each follow-up visit.

NCT ID: NCT01519206 Completed - Skin Laxity Clinical Trials

Lifting and Tightening of the Face and Neck Following an Increased Density Treatment

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

The purpose of this study is to evaluate the Ulthera® System for obtaining lift and tightening of the cheek tissue, reduction of jowling, and improving jawline definition and/or submental skin laxity when increased density treatment is applied.