Gene Expression Following Ultherapy® Treatment

Status Terminated

Clinical Trial Summary

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.

Clinical Trial Description

This is a prospective, multi-center, pilot clinical trial to evaluate the molecular changes following an Ultherapy® treatment. Subjects will be randomized to one of five treatment groups and, based on study group assignment, will receive one single-side Ultherapy® treatment at varying timepoints prior to an already planned facelift procedure. Treatment will be delivered to the pre-auricular region on one side of the face; the contralateral side will serve as control. During an already planned facelift procedure, treated and non-treated resected tissue will be obtained for analysis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02441036
Study type	Interventional
Source	Merz North America, Inc.
Contact
Status	Terminated
Phase	N/A
Start date	May 1, 2015
Completion date	August 18, 2016

View Details

See also
Status	Clinical Trial	Phase
Active, not recruiting	`NCT06140628` - A 28-day Clinical Study on Facial Skin Rejuvenation	N/A
Completed	`NCT01971736` - Efficacy of Long Pulsed 1064nm Laser for Facial Skin Tightening	N/A
Completed	`NCT01713985` - Feasibility Study: Evaluation of Ulthera Versus Thermage for Treating the Face and Neck	N/A
Completed	`NCT01708252` - Feasibility Study: Treatment of Post-surgery and Surgery Naive Patients Who Failed to Respond to a Previous Ulthera Treatment	N/A
Completed	`NCT01708382` - Feasibility Study: Lifting and Tightening of the Elbows	N/A
Completed	`NCT01713998` - Treatment of the Face and Neck With Lower Ulthera System Energy Settings	N/A
Completed	`NCT04296201` - Evaluation of the Immediate Effect and Safety of DMA™ Novel Muscle Stimulation Technology	N/A
Completed	`NCT06000839` - A Safety and Effectiveness Study of CELLBOOSTER® Lift (Stabilized Booster Complex Using CHAC Technology)	N/A
Completed	`NCT06366503` - Evaluating Procedure Pairing of a Post-Procedure Cream Versus a Comparator in Patients Treated With Fractional Ablative CO2 Laser for Facial Rejuvenation	N/A
Completed	`NCT05929625` - Radiofrequency and Ultrasound for Improvement of Skin Laxity and Wrinkles: Efficacy and Safety Evaluation	N/A
Terminated	`NCT01713569` - Feasibility Study: Histological Characterization After Treatment With the Ulthera® System	N/A
Completed	`NCT01519934` - A Retrospective Study to Evaluate the Effectiveness of the Ulthera System	N/A
Completed	`NCT05605691` - Post-Market Lower Eyelid Treatment With Renuvion in Greece	N/A
Completed	`NCT04477187` - Clinical Assessment of Skin Tightening and Contour Change of Submental Tissue Using Bipolar Radiofrequency Microneedling	N/A
Completed	`NCT05590364` - Aesthetic Performance and Tolerance of an Injective Intradermal Treatment for the Skin Roughness and Laxity of Back of the Hands	N/A
Active, not recruiting	`NCT06243744` - Histological Evaluation of Human Skin Bx to Assess the Effects of APR Tx as an Adjunct Procedure in Facelift Surgery	N/A
Completed	`NCT04146584` - Safety and Efficacy of SofWave Treatment to Lift Lax Tissue in the Submental and Neck Zones and to Lift the Eyebrow	Phase 2
Recruiting	`NCT05750901` - Evaluation of Fractional Ablative Laser Treatment for Skin Conditions	N/A
Completed	`NCT04721600` - Evaluation of the Evoke Radiofrequency Device for Improvement of Skin Appearance	N/A
Recruiting	`NCT06157567` - Clinical Feasibility Study to Evaluate the Safety and Performance of the Profound Matrix System	N/A