Search clinical trials for: Ulthera™ System

Total 81155 results

Ulthera, Inc

Completed

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

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Lifting and Tightening Neck Skin in Patients

Skin Laxity

United States
Ulthera, Inc

Completed

Histological Analysis Following Ulthera System Treatment for Hyperhidrosis

Hyperhidrosis

United States
Ulthera, Inc

Completed

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

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Lifting and Tightening of the Elbows

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Ulthera Treatment of the Buttocks and Thighs

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Ulthera® System for the Treatment of Moderate to Severe Facial Acne

Facial Acne

United States
Ulthera, Inc

Terminated

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

Wrinkles | Skin Laxity | Rhytids

United States
Ulthera, Inc

Completed

Evaluation of the Ulthera System for the Treatment of the Decolletage

Chest Wrinkles

United States
Ulthera, Inc

Completed

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

Skin Laxity

United States
Ulthera, Inc

Completed

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

Skin Laxity | Skin Crepiness

United States
Ulthera, Inc

Completed

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

Skin Laxity

United States
Ulthera, Inc

Completed

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

Wrinkles | Skin Laxity

United States
Ulthera, Inc

Completed

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

Skin Laxity of the décolleté

United States
Ulthera, Inc

Terminated

A Study of the Ulthera® System for the Treatment of Axillary Hyperhidrosis

Primary Axillary Hyperhidrosis

United States
Ulthera, Inc

Completed

Feasibility Study: Safety and Efficacy of the Ulthera® System for Treatment of Axillary Hyperhidrosis

Hyperhidrosis

United States
Ulthera, Inc

Terminated

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

Skin Laxity

United States
Ulthera, Inc

Completed

Evaluation of the Ulthera® System for Treatment of the Brachia

Brachial Ptosis

United States
Ulthera, Inc

Completed

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

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Ulthera System for the Treatment of Rosacea

Erythematotelangiectatic Rosacea

Canada
Ulthera, Inc

Completed

Ultherapy for Buttock Lift

Buttock Ptosis

United States
Ulthera, Inc

Completed

Evaluation of the Effectiveness and Safety of the Ulthera™ System for the Treatment of Wrinkles Around the Eyes

Periorbital Wrinkles

United States
Ulthera, Inc

Completed

Ulthera® System for Treating Axillary Hyperhidrosis

Primary Axillary Hyperhidrosis

United States
Ulthera, Inc

Completed

Feasibility Study: Ulthera® System for the Treatment of Axillary Hyperhidrosis

Hyperhidrosis

United States
Ulthera, Inc

Completed

Ultherapy for the Treatment of Spider Veins on the Legs

Spider Veins | Telangiectasia

United States
Ulthera, Inc

Completed

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

Skin Laxity

United States
Ulthera, Inc

Completed

Reducing Wrinkles Around the Eyes Using the Ulthera® System

Periorbital Wrinkles

United States
Ulthera, Inc

Completed

Ultherapy® for the Treatment of Erythematotelangiectatic Rosacea

Rosacea | Erythematotelangiectatic Rosacea

United States, Canada
Ulthera, Inc

Completed

Lifting and Tightening of the Face and Neck Utilizing the Ulthera® System

Facial and Neck Skin Laxity

United States
Ulthera, Inc

Terminated

Simulines Non-Inferiority Pivotal Study

Skin Laxity

United States
Ulthera, Inc

Terminated

Gene Expression Following Ultherapy® Treatment

Skin Laxity

United States
Ulthera, Inc

Completed

Ultherapy® for the Treatment of Acne Scars

Acne Scars | Atrophic Acne Scars

United States
Ulthera, Inc

Terminated

Peri-orbital and Peri-oral Wrinkle Reduction Trial

Peri-oral Wrinkles | Peri-orbital Wrinkles

United States
Seoul National University Hospital
Ministry of Health & Welfare, Korea

Completed

Safety and Efficacy Evaluation of Ultherapy™ System in Aging Hand

Wrinkles

Korea, Republic of
Ulthera, Inc

Completed

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

Skin Laxity

United States
Seoul National University Hospital
Ministry of Health & Welfare, Korea

Completed

Clinical Trial to Evaluate Safety and Efficacy of Ultherapy™ System for Lifting Skin on the Neck

Wrinkles

Korea, Republic of
Ulthera, Inc

Completed

Ultherapy™ Treatment Following Sculptra® Treatment

Skin Laxity

United States
Ulthera, Inc

Completed

Evaluation of the Ulthera System for Treating Axillary Hyperhidrosis (ULT-218)

Axillary Hyperhidrosis

Germany
Ulthera, Inc

Terminated

Feasibility Study: Evaluation of the Ulthera® System for Improvement of Surgical Scars.

Surgical Scar

United States
Ulthera, Inc

Completed

Feasibility Study: Evaluation of the Treatment of Striae Using Ultherapy® in Combination With Laser Treatment

Scars | Striae

United States
Ulthera, Inc

Completed

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

Skin Laxity

United States
Sanford Health

Suspended

Direct Resuscitation of the Open Peritoneum (SH DROP)

Abdomen, Acute | Wound Surgical | Wound; Abdomen

United States
Ulthera, Inc

Completed

Lifting and Tightening of the Face in Subjects With Skin of Darker Color

Facial Skin Laxity

United States
Deutsches Herzzentrum Muenchen

Recruiting

PROTECT TAVI - Prospective Randomized Outcome Study in TAVI Patients Undergoing Periprocedural Embolic Cerebral Protection With the Sentinel™ Device (PROTECT)

Cerebral Embolization During TAVI Using Balloon-expandable vs. Self-expandable Valves

Germany
Ulthera, Inc

Completed

Feasibility Study: Heavy Water Tissue Labeling Protocol

Skin Laxity

United States
Centro Cardiologico Monzino

Unknown

Role of the Type of Carotid Stent and Cerebral Protection on Cerebral Microembolization During Carotid Artery Stenting. A Randomized Study Comparing Carotid Wallstent vs Roadsaver® Stent and Distal vs Proximal Protection.

Carotid Stenosis

Italy
Medtronic Cardiovascular
Medtronic

Completed

The Medtronic CoreValve™ Evolut R™ CE Mark Clinical Study

Aortic Stenosis

New Zealand, United Kingdom, Australia
Boston Scientific Corporation

Withdrawn

iNod™ Ultrasound-Guided Needle Biopsy System Study

Multiple Pulmonary Nodules | Solitary Pulmonary Nodule | Biopsy, Fine-Needle

United States
Medtronic Cardiovascular

Completed

FORWARD PRO Study Interventional Post-market Study With the Evolut™ PRO System

Aortic Valve Stenosis

Netherlands, France, Italy, Germany, Spain, Denmark, Belgium, United Kingdom, Slovenia, Finland, Austria, Israel, Norway, Switzerland
CereVasc Inc
AlvaMed, Inc.; Simplified Clinical Data Systems, LLC; Bioscience Consulting,...

Recruiting

The ETCHES I Study (Endovascular Treatment of Communicating Hydrocephalus With an Endovascular Shunt) (ETCHES I)

Hydrocephalus | Hydrocephalus, Communicating

Argentina

3

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