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Lipolysis clinical trials

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NCT ID: NCT05507528 Completed - LIPOLYSIS Clinical Trials

Evaluation of the Safety and Efficacy of REBORN System for Lipolysis Treatment

Start date: June 30, 2022
Phase: N/A
Study type: Interventional

The Lightfective ReBorn System is intended for non-invasive lipolysis of the flanks in individuals with a Body Mass Index (BMI) of 30 or less. The device is intended to affect the appearance of visible fat bulges in the flanks.

NCT ID: NCT04881175 Terminated - Lipolysis Clinical Trials

Histological Study on Safety and Efficacy of a RF Device Flexible Applicator for Non-Invasive Lipolysis

Start date: February 9, 2021
Phase: N/A
Study type: Interventional

This is a prospective, open-labeled, non-randomized, multi-center clinical study to collect efficacy data on the TempSure FlexSure applicator for fat lipolysis.

NCT ID: NCT03721185 Completed - Physical Activity Clinical Trials

Efficacy of a Lipolytic Cream in an Overweight and Obesity Treatment

Start date: June 1, 2016
Phase: N/A
Study type: Interventional

The coadyouvant efficacy of a combination of cosmetics ingredients in the form of a lipolytic cream with hypocaloric diet and physical activity were assessed and compared with with hypocaloric diet and physical activity for overweight and obesity treatment in patients.

NCT ID: NCT03675464 Recruiting - Obesity Clinical Trials

Study of Human Adipose Tissue (LOSHAT)

LOSHAT
Start date: September 20, 2018
Phase:
Study type: Observational

The investigators will study the influence of initial fat cell size/number and adipose function (in particular lipolysis) on weight development over very long time periods (years). By comparing investigations of fat biopsies or blood samples obtained at baseline, the investigators will determine the association between adipose morphology/function and changes in weight or development of metabolic complications (e.g. metabolic syndrome, glucose intolerance, type 2 diabetes, dyslipidemia and hypertension).

NCT ID: NCT03588702 Completed - Lipolysis Clinical Trials

RF and PEMF Following Liposuction

Start date: July 2, 2018
Phase: N/A
Study type: Interventional

The Venus Legacy LB2 Body applicator is intended for circumference reduction treatment by reducing fat cell size and enhancing collagen synthesis as the result of thermal and non-thermal collagen stimulation. This is an open-label, evaluator-blind study of the safety and performance of radiofrequency (RF) and pulsed electromagnetic field (PEMF) therapy following liposuction. The study will enroll up to 50 male and female subjects requesting treatment of the back, flanks and/or thighs to improve appearance following liposuction. Subjects will receive a total of six study treatments to one side of their body (back, flanks and/or thighs) at one week intervals. Subjects will be followed up at one month after their last study treatment. Treatment outcomes will be compared to the non-treated side.

NCT ID: NCT03171051 Terminated - Lipolysis Clinical Trials

LED Device for Non-Invasive Lipolysis

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

This study is being conducted to evaluate the ability of a light emitting diode (LED) study device's ability to raise the temperatures on flank tissue to a similar level compared to an approved laser device (SculpSure by Cynosure). Laser treatments have been shown to reduce fat in the flanks by heating the fat cells and causing them to burst. The contents of the cells are then cleared naturally by the body.

NCT ID: NCT03062163 Completed - Lipolysis Clinical Trials

Efficacy and Safety of Resveratrol and Lipoic Acid Transdermal Patch for Lipolysis in Overweight Volunteers

Start date: January 23, 2017
Phase: N/A
Study type: Interventional

To evaluate the lipolysis effect of resveratrol and lipoic acid transdermal patch in overweight volunteers

NCT ID: NCT01177787 Completed - Cryotherapy Effect Clinical Trials

Clinical Efficacy of Cryolipolysis on the Fat of Thigh in Korean Women

Start date: July 1, 2010
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the clinical efficacy of reduction of local fat on ipsilateral thigh through cryolipolysis (zeltiq) and controlateral thigh using by amplitude modulated frequency (conventional) method.