Performance and Safety of the Lipo-transfer Cannulas in Patients Underlying Lipofilling Treatment

Last updated: July 31, 2024
Sponsor: Aesthetic Group
Overall Status: Completed

Phase

N/A

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT06089759
LIPOTRANSFER
  • Ages > 18
  • All Genders

Study Summary

The purpose of this post-market clinical follow up study is to assess the safety and performance of Aesthetic Group cannulas. The study will evaluate the outcome of the Aesthetic Group cannulas range over a period of 1 month after intervention.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patient age ≥ 18 years at intervention

  • Patient who will undergo a lipofilling treatment with at least one cannula ofAesthetic Group

  • Patient informed of his/her participation and willing to participate in the study.

  • Patient able to read, write and understand French.

Exclusion

Exclusion Criteria:

  • Patient deprived of freedom, under guardianship/curatorship or placed under judicialprotection

  • Patient unable to follow study procedures

  • Patient with hematologic abnormalities, prior radiotherapy or chemotherapy

  • Chronic use of medicines or drugs

  • Patient with diabetes mellitus

  • Patient with connective tissue diseases, any type of fat tissue disorder (lipodystrophy)

  • Patient with bleeding disorders; immune deficits; heart, liver, and kidneyinsufficiency

  • Patient with allergies to local anaesthetics

  • Patient with pacemaker and serious heart rhythm disorders

  • Pregnant and breastfeeding women

Study Design

Total Participants: 108
Study Start date:
August 30, 2023
Estimated Completion Date:
July 31, 2024

Connect with a study center

  • Clinique Pasteur

    Brest, 29200
    France

    Site Not Available

  • Clinique Phenicia

    Marseille, 13005
    France

    Site Not Available

  • Clinique Eiffel

    Paris, 75116
    France

    Site Not Available

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