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CompletedNCT03769649

Clinical Evaluation of CelluTite Treatment

Clinical Evaluation of Safety and Efficacy of the CelluTite Treatment

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
15 (actual)
Sponsor
InMode MD Ltd. · Industry
Sex
Female
Age
18 Years – 70 Years
Healthy volunteers
Accepted

Summary

This prospective study is intended to evaluate the CelluTite RFAL handpiece combined with Morpheus8 handpiece for the treatment of cellulite.

Detailed description

The study will evaluate the safety and efficacy of cellulite treatment using two hand pieces: * The CelluTite - based on a minimally invasive, temperature-controlled Radiofrequency-assisted lipolysis (RFAL) technology. RF energy is applied using a handpiece with 2 electrodes: internal active electrode with spatula-shaped tip and external electrode. * The Morpheus8 - designed to deliver RF energy to the skin surface in a fractional manner via an array of 24-electrode pins.

Conditions

Interventions

TypeNameDescription
DEVICECelluTiteCelluTite: Radiofrequency-assisted lipolysis (RFAL) Morpheus8: Fractional RF

Timeline

Start date
2018-11-12
Primary completion
2020-01-17
Completion
2020-01-17
First posted
2018-12-07
Last updated
2022-06-08
Results posted
2021-02-16

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03769649. Inclusion in this directory is not an endorsement.

Clinical Evaluation of CelluTite Treatment (NCT03769649) · Clinical Trials Directory