The Co-Op @ HeartWorks for Congenital Heart Disease

This study, called The Co-Op @ HeartWorks, is creating a registry (a database) of people with Congenital Heart Disease (CHD), which are heart problems present at birth. It's not testing a specific treatment, but rather gathering information about the medical journeys of individuals with CHD. This information will help researchers design better future studies and treatments that truly meet the needs of the CHD community. You can join if you are an adult with CHD, a caregiver of a child with CHD, or a family member of someone who had CHD and has passed away. The goal is to build this registry over 25 years to guide future research. The current recruitment status is unclear.

Study design
This is an observational study aiming to enroll 500 participants. It is not a traditional clinical trial testing a specific intervention.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be part of a registry that aims to collect data for 25 years.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06469918

The Co-Op @ HeartWorks

Recruiting
Not specifiedAges 0+Observational
HeartWorks, Inc.
~500 participants
Updated 2025-10-07 on ClinicalTrials.gov

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Registry of individuals with CHD to plan and recruit for future interventional trials in Congenital Heart Defects/Disease
Measured over 25 years
Congenital Heart Disease

NCT06469918

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • HeartWorks, Inc.

    Rochester, Minnesotastudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

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Eligibility criteria

Inclusion

Adult with a congenital heart defects/disease
Caregiver of a minor with a congenital heart defect/disease
Authorized family member of a now deceased person with congenital heart defect/disease
  • Registry of individuals with CHD to plan and recruit for future interventional trials in Congenital Heart Defects/Disease25 years