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

NCT06089759 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 108

Last updated 2024-08-01

No results posted yet for this 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.

Conditions

  • Lipodystrophy
  • Deformities

Sponsors & Collaborators

  • EVAMED

    collaborator OTHER

  • Aesthetic Group

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-30
Primary Completion
2024-07-01
Completion
2024-07-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06089759 on ClinicalTrials.gov