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

NCT06932081 · Leiden University Medical Center
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Official title
Adult Congenital Heart Disease International EValuation of the Effectiveness of SGLT2i (ACHIEVE-SGLT2i) Registry
About this study
In the adult congenital heart disease (ACHD) population, heart failure currently represents the main cause of morbidity and mortality. The etiology of ACHD-related heart failure is heterogenous, and there is limited evidence for pharmacological treatment options for this population. Sodium-glucose cotransporter 2 inhibitors (SGLT2i) are a novel pillar in the treatment of conventional LV heart failure. SGLT2i have been shown to reduce the risk of worsening heart failure and cardiovascular-related death in patients with LV heart failure. While the exact mechanisms of action are still to be elucidated, SGLT2i seem to address heart failure by targeting several pathways. These include but are not limited to; a decrease in renin-angiotensin and sympathetic nervous system activation, a decrease in pressure overload-induced myocardial fibrosis, reverse cardiac remodeling, and improvement in myocardial energetics. Given the compelling evidence on the effectiveness of SGLT2i over a broad range of cardiac dysfunction and initial promising reports of its utilization in the field of ACHD, SGLT2i deserve further exploration in the group of ACHD patients. This real-world, international registry aims to evaluate the current experience with SGLT2i in ACHD patients by investigating the prescription patterns, safety, tolerability, and potential beneficial effects on heart failure-related outcomes. Project design: Data of all ACHD patients who were started on an SGLT2i will be collected in a real-world, international registry. Only data resulting from routine clinical care will be collected from the electronic health records at the participating centers, and participants will not undergo any interventions for this project. Data will be collected from 1 year before starting with the SGLT2i to most recent follow-up after starting with the SGLT2i, to evaluate if SGLT2i therapy halts the progression of clinical deterioration in ACHD patients with heart failure and can improve heart failure-related outcomes.
Eligibility criteria
Inclusion Criteria: * Congenital heart defect. * Age ≥ 18 years. * Initiated on treatment with an SGLT2i. Exclusion Criteria: \- No consent for data collection.
Study design
Enrollment target: 400 participants
Age groups: adult, older_adult
Timeline
Starts: 2023-01-01
Estimated completion: 2027-12-31
Last updated: 2026-02-13
Interventions
Drug: SGLT2 inhibitors
Primary outcomes
  • Prescription patterns (Baseline information.)
Sponsor
Leiden University Medical Center · other
Contacts & investigators
ContactRalph M.L. Neijenhuis, MD · contact · r.m.l.neijenhuis@lumc.nl · +31 71 5262020
ContactBjörn N. Westdorp, MD · contact · b.n.westdorp@lumc.nl · +31 71 5262020
InvestigatorAnastasia D. Egorova, MD PhD · principal_investigator, Leiden University Medical Center
All locations (11)
Johns Hopkins UniversityRecruiting
Baltimore, Maryland, United States
Helen DeVos Children's HospitalRecruiting
Grand Rapids, Michigan, United States
Mount Sinai Fuster Heart HospitalRecruiting
New York, New York, United States
Heart Center Duisburg (Evangelical Hospital Niederrhein)Recruiting
Duisburg, Germany
Leiden University Medical Center (LUMC)Recruiting
Leiden, South Holland, Netherlands
Amsterdam University Medical CenterRecruiting
Amsterdam, Netherlands
University Medical Center UtrechtRecruiting
Utrecht, Netherlands
Zan Mitrev ClinicRecruiting
Skopje, North Macedonia
University Hospital of WalesRecruiting
Cardiff, United Kingdom
Golden Jubilee University National HospitalRecruiting
Glasgow, United Kingdom
Barts Heart CentreRecruiting
London, United Kingdom
Adult Congenital Heart Disease International EValuation of the Effectiveness of SGLT2i Registry · TrialPath