πŸ›οΈ Verified NIH Record β€’ Updated 2026-08-27

Starlight Cardiovascular Lifeline Ductus Arteriosus Stent IDE Study (NCT07114718)

🟒 Recruiting Observational / Diagnostic βš™οΈ Medical Device Protocol Sponsor: Starlight Cardiovascular Inc

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

Starlight Cardiovascular, Inc. is sponsoring a prospective, multi-center, study to evaluate safety and effectiveness of the Lifeline Ductus Arteriosus Stent System. The study device is a stent that is designed to maintain patency of the Ductus Arteriosus for children who need blood flow through that part of the heart.

Who can join: Review the eligibility criteria below.

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

Age range: 1 Minute to 6 Months

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 (9 Sites)

  • UCLA Mattel Children's β€” Los Angeles, California
  • Leland Stanford Junior University β€” Stanford, California
  • Children's Hospital Colorado β€” Aurora, Colorado
  • Boston Children's Hospital β€” Boston, Massachusetts
  • Cincinnati Children's Hospital Medical Center β€” Cincinnati, Ohio
  • Nationwide Children's Hospital β€” Columbus, Ohio
  • Children's Hospital of Philadelphia β€” Philadelphia, Pennsylvania
  • Texas Children's Hospital - Baylor College of Medicine β€” Houston, Texas
  • Seattle Children's Hospital β€” Seattle, Washington

πŸ“ž Contact the Study Coordinator

Phone: (734) 709-2080

Email: marybeth.tate@globalmedicaldeviceconsultants.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.

More studies in Congenital Heart Disease

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†—