Prospective WCD Post CABG Registry (CABG Registry)
Recruiting
Observational Study
Cardiomyopathy Ischemic
Cardiomyopathies
Cardiovascular Diseases
Heart Disease, Ischemic
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 910 (estimated)
- Sponsor
- Zoll Medical Corporation · Industry
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About This Trial
The primary objective is to observe the rate of recovery of ventricular function (EF\>35%) after first-time coronary artery bypass graft surgery in patients who were prescribed the wearable cardioverter defibrillator (WCD) post-surgery prior to being discharged after hospitalization as part of standard clinical care.
Trial Locations
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Eligibility Criteria
Inclusion Criteria
* Patient underwent first-time CABG surgery \<10 days before enrollment.
* Patient is prescribed WCD for a primary reason of HF with reduced EF \< 35% measured after surgery but before hospital discharge.
* Patient is ≥18 years old
Exclusion Criteria:
* Patients having combinat…
Contacts