πŸ›οΈ Verified NIH Record β€’ Updated 2026-08-06

Autus Valve Continued Access Study (CAS) (NCT07466745)

Autus Size-Adjustable Valve for Surgical Pulmonary Valve Replacement Continued Access Study

🟒 Recruiting Observational / Diagnostic βš™οΈ Medical Device Protocol Sponsor: Edwards Lifesciences

🩺 Plain-English Summary (8th-Grade Level)

Prospective, single-arm, multi-center, continued access study of the Autus Size-Adjustable Valve in pediatric patients aged 18 months to 16 years requiring surgical pulmonary valve replacement. The Autus Valve may be expanded pre-implant to match the subject's body size. Subjects will be evaluated prior to the Autus Valve implant procedure, immediately post-implantation, at hospital discharge, 30 days, 6 months, and annually through 10 years. The Autus Valve may be expanded post-implant via transcatheter balloon dilation to accommodate growth of the subject.

Who can join: Review the eligibility criteria below.

Location: Children's Hospital Los Angeles β€” Los Angeles, California

Age range: 18 Months to 16 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

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

πŸ“ All Participating Trial Locations (10 Sites)

  • Children's Hospital Los Angeles β€” Los Angeles, California
  • Children's Hospital Colorado β€” Aurora, Colorado
  • Children's Healthcare of Atlanta β€” Atlanta, Georgia
  • Boston Children's Hospital β€” Boston, Massachusetts
  • University of Michigan - Mott Children's Hospital β€” Ann Arbor, Michigan
  • Columbia University Irving Medical Center/New York Presbyterian Morgan Stanley Children's Hospital β€” New York, New York
  • Duke University β€” Durham, North Carolina
  • Nationwide Children's Hospital β€” Columbus, Ohio
  • University of Utah - Intermountain Primary Children's Hospital β€” Salt Lake City, Utah
  • Seattle Children's Hospital β€” Seattle, Washington

πŸ“ž Contact the Study Coordinator

Phone: (949) 250-2500

Email: Jennie_Wurgler@edwards.com

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

πŸ’° 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 Β§ 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.

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πŸ’‘ 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.
πŸ›οΈ View Official NIH Record β†—