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Assessment of Cellular and Tissue Characteristics in Lipoaspirates Stirred by VorFat

A

Alma Lasers

Status

Withdrawn

Conditions

Laser Assisted Liposuction

Treatments

Device: LipoLife system

Study type

Interventional

Funder types

Industry

Identifiers

NCT05016674
ALM-Lipo-VorFat-21-013

Details and patient eligibility

About

Single-center, prospective, open-label study. The study aims to assess the structure and viability of fat collected during the LipoLife liposuction procedure

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Subjects scheduled to undergo abdominal w/wo flanks laser-assisted liposuction surgery and are willing to donate the harvested adipose tissue for the study assessment.
  2. Between 18 and 70 years of age.
  3. Estimated fat harvesting of at least 300 milliliters.
  4. Provided written Informed Consent.

Exclusion criteria

  1. Pregnant or intending to become pregnant during the course of study.
  2. Current smoker.
  3. Presence of known malignancy.
  4. Active infection in the treatment area.
  5. History of autoimmune disorder (e.g., Systemic Lupus Erythematosus [SLE]).
  6. History of connective, metabolic, or atrophic skin disease.
  7. History of keloid scarring.
  8. Chronic use (>7 consecutive days) of anticoagulants (such as aspirin) or NSAIDs within 15 days before enrollment.
  9. Subjects with immune system diseases.
  10. Any other reason that in the opinion of the investigator, prevents the subject from participating in the study or compromises the subject safety.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

Laser-assisted liposuction
Experimental group
Description:
Laser-Assisted Liposuction with the LipoLife system.
Treatment:
Device: LipoLife system

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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