Clinical Trials Logo

Cellulite clinical trials

View clinical trials related to Cellulite.

Filter by:

NCT ID: NCT01671839 Completed - Clinical trials for Gynoid Lipodystrophy

Study of the Cabochon System for Improvement in the Appearance of Cellulite

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

The purpose of this study is to evaluate the safety and effectiveness of the Cabochon System for the improvement in the appearance of cellulite.

NCT ID: NCT01518907 Completed - Cellulite Clinical Trials

The Safety, Effectiveness, and Pharmacokinetics of AA4500 for the Treatment of Edematous Fibrosclerotic Panniculopathy (Commonly Known as Cellulite)

Start date: January 2012
Phase: Phase 1
Study type: Interventional

This study will evaluate the safety, effectiveness, pharmacokinetics, and immunogenicity of AA4500 at increasing doses and concentrations in the treatment of adult women with cellulite.

NCT ID: NCT01234259 Completed - Clinical trials for Circumference Reduction

Evaluation of Safety and Efficacy of Using Venus Freezeā„¢ (MP)2 V2 System for Wrinkles Rhytides and Cellulite Treatment

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

Skin aging is a multifactorial process involving the 3 layers of the skin: Epidermis, dermis and hypodermis. Radio-frequency (RF) devices have been used for many years for a variety of surgical applications. The energy delivery systems of these established monopolar devices used a 'conductive coupling' delivery system in which energy is concentrated at the periphery of the electrode. Venus Concept has developed the Venus Freeze (MP)2 V2 system for wrinkles, rhytides and temporary cellulite and circumference reduction treatments. While treating wrinkles rhytides and cellulite, the treatments creates enough thermal effect to induce collagen remodeling with no ablative thermal damage in the epidermis or dermis.

NCT ID: NCT01209767 Completed - Cellulite Clinical Trials

Cryolipolysis and Subcision for Treatment of Cellulite

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

This study intended to investigate and compare the changes that may occur in response to cryolipolysis (localized cool exposure) and subcision (surgical technique) on cellulite. The cryolipolysis cooling device used is FDA approved for skin cooling, but still investigational in the treatment of cellulite. It has previously been used for fat reduction on love handles or back fat. During cryolipolysis, the system drew fat tissue into an applicator then exposes the extracted fat tissue to cold temperatures. The cold exposure caused fat cells to die, with the goal to decrease the raised areas of cellulite. Subcision is a process used to treat scars left behind by acne or other skin diseases and has been noted to improve moderate to severe cellulite. Subcision is a simple surgical procedure that is performed by inserting a specially designed needle under the skin after local numbing medication is injected. The needle is moved in a repetitive motion parallel to the skin to separate the surface tissue from the deeper scar tissue with the goal to improve the dimpling caused by these tissues sticking together. This study was a pilot study designed to determine feasibility of these procedures.

NCT ID: NCT00953160 Terminated - Cellulite Clinical Trials

Radio Frequency (RF) Device for Reduction in Size of Localized Areas of the Body

Start date: April 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the Cutera radio frequency (RF) device for the new indication of reduction in size of localized areas of the body.

NCT ID: NCT00947414 Completed - Microcirculation Clinical Trials

Cellulite and Extracorporeal Shock Wave

Start date: June 2009
Phase: N/A
Study type: Interventional

Hypothesis: The combination of extracorporeal shockwave and a daily gluteal muscle strength programme is superior to the gluteal muscle strength programme alone in cellulite. Study design: Randomized-controlled trial Analysis: Intention-to-treat Outcome parameters: a) Photo, b) Nürnberger Score, c) circumference measurements, d) capillary blood flow, e) tissue oxygen saturation, f) postcapillary venous blood flow Intervention: Extracorporeal shock wave for six sessions with 2000 impulses at both gluteal and thigh regions plus a specific gluteal strength exercise training Follow-up: 12 weeks

NCT ID: NCT00399854 Completed - Cellulite Clinical Trials

Evaluation of the Efficacy of Endermologie in Treatment of Cellulite and Body Contouring

Start date: March 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to perform a clinical assessment of the efficacy of the device DHERMIA® (Industra Mecânica Fina Ltda)in the treatment of cellulite and body contouring

NCT ID: NCT00399828 Terminated - Cellulite Clinical Trials

Evaluation Of The Efficacy and Safety Of Tri-ActiveTM In Treatment Of Cellulite

Start date: August 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the efficacy of device TRI-ACTIVETM (DEKA M.E.L.A., Itália)in the treatment od cellulite and body contouring.

NCT ID: NCT00261144 Not yet recruiting - Cellulite Clinical Trials

Collagenase in the Treatment of Cellulite

Start date: February 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if collagenase injection will reduce or eliminate the appearance of cellulite of the thigh.