Status: Recruiting
Prospective WCD Post CABG Registry (CABG Registry)
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.
Participants needed: 910
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Zoll Medical CorporationUpdated: Nov 4, 2024Locations: 4Duration: 12 Months
Eligibility criteria
Patient underwent first-time CABG surgery <10 days before enrollment. [+2]
Patients having combination CABG surgery with heart valve repair. [+3]