Ambulatory Surgical Center Implantable Cardioverter-Defibrillator Outcomes Registry

Description

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.

Conditions

Arrhythmia

Study Overview

Study Details

Study overview

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.

Ambulatory Surgical Center Implantable Cardioverter-Defibrillator Outcomes Registry

Ambulatory Surgical Center Implantable Cardioverter-Defibrillator Outcomes Registry

Condition
Arrhythmia
Intervention / Treatment

-

Contacts and Locations

Lehi

Cardio Surgical Partners, LLC, Lehi, Utah, United States, 84043

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

  • * Physician recommendation to receive the implant in an Ambulatory Surgical Center (ASC)
  • * N/A

Ages Eligible for Study

to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

QuesGen Systems Inc,

Study Record Dates

2028-08-24