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Retrospective Evaluation of Cellulite of Laxity Treatment Using Body Tite

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Status

Completed

Conditions

Cellulite

Treatments

Device: BodyTite

Study type

Observational

Funder types

Industry

Identifiers

NCT04419454
DO609568A

Details and patient eligibility

About

Retrospective Evaluation of Cellulite of Laxity Treatment Using Body Tite

Full description

The purpose of this preliminary report is to retrospectively evaluate this novel treatment approach to improve the appearance of cellulite on the thighs and buttocks by tightening the SFS using RFAL.

Enrollment

10 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • age ≥ 18years of age at the time of procedure

    • patients with localized lipodystrophy in the medial or lateral thigh, and visible cellulite of laxity in the lower extremity or buttocks
    • BodyTite treatments performed from January 2018 - May 2019 for Cellulite indication

Exclusion criteria

  • active infection, collagen disorders, immunocompromised state, medications that mitigate inflammatory response, and propensity for keloid/hypertrophic scaring. o BodyTite treatments performed from March 2018 - May 2019 for lipodystrophy and cellulite of laxity

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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