๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-02-11

Adult Congenital Heart Disease International EValuation of the Effectiveness of SGLT2i Registry (NCT06932081)

Adult Congenital Heart Disease International EValuation of the Effectiveness of SGLT2i (ACHIEVE-SGLT2i) Registry

๐ŸŸข Recruiting Interventional Protocol ๐Ÿ“Š Observational Clinical Research Sponsor: Leiden University Medical Center

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

This real-world, international registry aims to evaluate the current experience with sodium-glucose cotransporter 2 inhibitors (SGLT2i) in adult congenital heart disease (ACHD) patients by investigating the prescription patterns, safety, tolerability, and potential beneficial effects on heart failure-related outcomes.

Who can join: Review the eligibility criteria below.

Location: Johns Hopkins University โ€” Baltimore, Maryland

Age range: 18 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 (11 Sites)

  • Johns Hopkins University โ€” Baltimore, Maryland
  • Helen DeVos Children's Hospital โ€” Grand Rapids, Michigan
  • Mount Sinai Fuster Heart Hospital โ€” New York, New York
  • Heart Center Duisburg (Evangelical Hospital Niederrhein) โ€” Duisburg,
  • Leiden University Medical Center (LUMC) โ€” Leiden, South Holland
  • Amsterdam University Medical Center โ€” Amsterdam,
  • University Medical Center Utrecht โ€” Utrecht,
  • Zan Mitrev Clinic โ€” Skopje,
  • University Hospital of Wales โ€” Cardiff,
  • Golden Jubilee University National Hospital โ€” Glasgow,
  • Barts Heart Centre โ€” London,

๐Ÿ“ž Contact the Study Coordinator

Phone: +31 71 5262020

Email: r.m.l.neijenhuis@lumc.nl

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†—