Clinical Trials Logo

Cellulite clinical trials

View clinical trials related to Cellulite.

Filter by:

NCT ID: NCT03329989 Completed - Cellulite Clinical Trials

Safety and Effectiveness of EN3835 in the Treatment of EFP in Women

Start date: November 17, 2017
Phase: Phase 2
Study type: Interventional

An open-label study of safety and effectiveness of EN3835 in the treatment of cellulite in adult women.

NCT ID: NCT03312946 Recruiting - Cellulitis Clinical Trials

Effect of Vibro-oscillatory Therapy for Improvement of Body Contour and Appearance of Cellulite.

Start date: October 13, 2017
Phase: N/A
Study type: Interventional

OBJECTIVE: To evaluate the efficacy of vibro-oscillatory therapy through an electromedical equipment in improving body contour and appearance of cellulite. SUBJECTS AND METHODS: A prospective and comparative longitudinal clinical study will be performed in 30 women with cellulitis. Patients will be submitted to data collection and evaluation and before and after vibration-oscillatory therapy. HYPOTHESES: Patients are expected to show improvement in body contour and cellulite after vibration-oscillatory therapy. STATISTICAL ANALYSIS: A descriptive analysis will be done before and after vibration-oscillatory therapy, with frequency tables for categorical and descriptive variables (mean, standard deviation, median, minimum and maximum values) for continuous or numerical variables. In order to compare the main variables between the groups and the collection times, the analysis of variance (ANOVA) for repeated measures will be used. Tukey's test will be used to compare the groups. The significance level adopted for the statistical tests will be 5% or p <0.05.

NCT ID: NCT03078647 Completed - Cellulite Clinical Trials

Profound Dermal and SubQ Cartridges for the Treatment of Cellulite

Start date: September 13, 2017
Phase: N/A
Study type: Interventional

Clinical Study to Evaluate the Performance of the Profound System for the Treatment of Cellulite.

NCT ID: NCT02942160 Completed - Cellulite Clinical Trials

EN3835 for the Treatment of Edematous Fibrosclerotic Panniculopathy (Commonly Known as Cellulite)

Start date: October 5, 2016
Phase: Phase 2
Study type: Interventional

A Phase 2, Open-Label Extension Study of EN3835 in the Treatment of Edematous Fibrosclerotic Panniculopathy (commonly known as Cellulite).

NCT ID: NCT02903459 Completed - Lordosis Clinical Trials

Analyze the Relationship Between the Density of Fat Tissue and Cellulite With the Lumbar Lordosis Degree

Start date: June 2016
Phase: N/A
Study type: Observational

The aim of this study is analyze the relationship between the density of visceral and subcutaneous fat and cellulite with the lumbar lordosis degree.

NCT ID: NCT02724644 Completed - Cellulite Clinical Trials

EN3835 for the Treatment of Edematous Fibrosclerotic Panniculopathy (Commonly Known as Cellulite)

Start date: February 2016
Phase: Phase 2
Study type: Interventional

The study will evaluate the safety, effectiveness, and immunogenicity of EN3835 in the treatment of adult women with Edematous Fibrosclerotic Panniculopathy (Commonly known as Cellulite).

NCT ID: NCT02489994 Active, not recruiting - Cellulite Clinical Trials

Performance of the ePrime System for Cellulite

Start date: October 2014
Phase: N/A
Study type: Interventional

Clinical Study to Evaluate the Performance of the ePrime System for the Treatment of Cellulite.

NCT ID: NCT02427698 Active, not recruiting - Cellulite Clinical Trials

Cyrolipolysis vs Cyrolipolysis and Subcision for Cellulite

Start date: August 2015
Phase: N/A
Study type: Interventional

This is a prospective randomized controlled study comparing the efficacy of cryolipolysis versus a combination of cryolipolysis and surgical subcision for the treatment of cellulite. The treatment sites are both outer thighs. One outer thigh will be randomized to receive one treatment of cryolipolysis, while the contralateral thigh will be assigned to receive the combination cryolipolysis plus surgical subcision. A live rating by a blinded dermatologist will evaluate the treatment and control areas using a cellulite severity scale at week 0 (before treatment) and at the 3-month follow up visit.

NCT ID: NCT02127723 Completed - Clinical trials for Cellulite of the Buttocks

(Macrolane VR30) in Buttocks Reshaping and contouringCellulite (Macrolane VR30) in Buttocks Reshaping and Contouring

Start date: April 2014
Phase: N/A
Study type: Interventional

The most common treatments today for enhancing the shape and size of the buttocks are transplantation of the patient's own body fat after liposuction and insertion of permanent implants. Macrolane VRF30 is a gel product based on hyaluronic acid which is a transparent slow-flowing gel. A similar hyaluronic-acid gel from the same manufacturer, Q-Med AB, has been used for many years for the treatment of facial wrinkles. By injecting Macrolane gel into the skin, the shape of the buttocks can be altered and their volume increased.

NCT ID: NCT01702259 Completed - Cellulite Clinical Trials

Study of the Effect of Low Level Laser Light Therapy on Reducing the Appearance of Cellulite in the Thighs and Buttocks.

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

The purpose of this study is to determine whether the application of green diode low level laser light therapy is effective in reducing the appearance of cellulite in the thighs and buttocks.