๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2024-12-20

Clinical Trial Assessing Human Placental Membrane Products and Standard of Care Versus Standard of Care in Nonhealing DFUs and VLUs (NCT06674980)

A Multicenter, Prospective, Randomized Controlled Modified Platform Trial Assessing the Efficacy of Human Placental Membrane Products and Standard of Care Versus Standard of Care Alone in the Management of Nonhealing Diabetic Foot Ulcers and Venous Leg Ulcers.

๐ŸŸข Recruiting Observational / Diagnostic ๐Ÿ“‹ Clinical Research Protocol Sponsor: C5 Biomedical

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

The purpose of the study is to evaluate the efficacy of multiple human placental membrane products and Standard of Care (SOC) versus SOC alone in the management of nonhealing diabetic foot ulcers (DFUs) and venous leg ulcers (VLUs) over 12 weeks using a modified platform trial design.

Who can join: Review the eligibility criteria below.

Location: Poirot Podiatry โ€” Metairie, Louisiana

Age range: 18 Years

๐Ÿงช Interventions in This Study

  • Standard of Care - DFU (OTHER)
  • AM/Single - DFU (OTHER)
  • AM/Double - DFU (OTHER)
  • Standard of Care - VLU (OTHER)
  • AM/Single - VLU (OTHER)
  • AM/Double - VLU (OTHER)

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 (1 Sites)

  • Poirot Podiatry โ€” Metairie, Louisiana

๐Ÿ“ž Contact the Study Coordinator

Phone: (888) 960-1343

Email: Brogers@serenagroups.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

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.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  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†—