๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2025-08-18

Clinical Feasibility Study to Evaluate the Safety and Performance of the Profound Matrix System (NCT06157567)

๐Ÿ”ต Active, Not Recruiting Observational / Diagnostic โš™๏ธ Medical Device Protocol Sponsor: Candela Corporation

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This is a non-randomized, multi-center, open-label clinical trial evaluating clinical feasibility treatments with the Profound Matrix system.

Who can join: Review the eligibility criteria below.

Location: Center for Morden Aesthetic Medicine โ€” Jacksonville, Florida

Age range: 18 Years to 75 Years

๐Ÿงช Interventions in This Study

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (6 Sites)

  • Center for Morden Aesthetic Medicine โ€” Jacksonville, Florida
  • Candela Institue for Excellence โ€” Marlborough, Massachusetts
  • Concierge Medical Arts โ€” Fayetteville, North Carolina
  • Gerrish MedEsthetics โ€” Vienna, Virginia
  • Waterfront Skin and Laser โ€” Vancouver,
  • Candela European Institue of Excellence โ€” Madrid,

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Skin Laxity clinical trials

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—