RecruitingNCT06932081

Adult Congenital Heart Disease International EValuation of the Effectiveness of SGLT2i Registry

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


Sponsor

Leiden University Medical Center

Enrollment

400 participants

Start Date

Jan 1, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • Congenital heart defect.
  • Age ≥ 18 years.
  • Initiated on treatment with an SGLT2i.

Exclusion Criteria1

  • \- No consent for data collection.

Interventions

DRUGSGLT2 inhibitors

Treatment with any type and dose of sodium-glucose cotransporter 2 inhibitor.


Locations(11)

Johns Hopkins University

Baltimore, Maryland, United States

Helen DeVos Children's Hospital

Grand Rapids, Michigan, United States

Mount Sinai Fuster Heart Hospital

New York, New York, United States

Heart Center Duisburg (Evangelical Hospital Niederrhein)

Duisburg, Germany

Leiden University Medical Center (LUMC)

Leiden, South Holland, Netherlands

Amsterdam University Medical Center

Amsterdam, Netherlands

University Medical Center Utrecht

Utrecht, Netherlands

Zan Mitrev Clinic

Skopje, North Macedonia

University Hospital of Wales

Cardiff, United Kingdom

Golden Jubilee University National Hospital

Glasgow, United Kingdom

Barts Heart Centre

London, United Kingdom

View Full Details on ClinicalTrials.gov

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NCT06932081


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