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Ambulatory Surgical Center Implantable Cardioverter-Defibrillator Outcomes Registry (ASC ICD Reg)

Q

QuesGen Systems

Status

Enrolling

Conditions

Arrhythmia

Study type

Observational

Funder types

Other
NETWORK

Identifiers

NCT03604133
2018-310 Cardiac Registry

Details and patient eligibility

About

The primary objectives for the registry is to evaluate the overall incidence of serious complications or adverse events for primary implants and replacement devices, and assess the cost and time efficiency for both physicians and patients. The Registry is a multi ASC data collection registry. Data collection will occur at the time of screening, implant, and 2 weeks after implant at the time of wound check.

Enrollment

500 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Physician recommendation to receive the implant in an Ambulatory Surgical Center (ASC)

Exclusion criteria

  • N/A

Trial design

500 participants in 1 patient group

Patients receiving ICD devices

Trial contacts and locations

1

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Central trial contact

Martin Jorgensen, PhD; Michael Jarrett, MBA

Data sourced from clinicaltrials.gov

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