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

Description

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.

Conditions

Adult Congenital Heart Disease, Congenital Heart Disease, Systemic Right Ventricle, Transposition of the Great Arteries, Congenitally Corrected Transposition of the Great Arteries, Fontan, Single Ventricle, Tetralogy of Fallot (TOF)

Study Overview

Study Details

Study overview

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.

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

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

Condition
Adult Congenital Heart Disease
Intervention / Treatment

-

Contacts and Locations

Baltimore

Johns Hopkins University, Baltimore, Maryland, United States, 21205

Grand Rapids

Helen DeVos Children's Hospital, Grand Rapids, Michigan, United States, 49503

New York City

Mount Sinai Fuster Heart Hospital, New York City, New York, United States, 10029

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

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

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Leiden University Medical Center,

Anastasia D. Egorova, MD PhD, PRINCIPAL_INVESTIGATOR, Leiden University Medical Center

Study Record Dates

2027-12-31