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

  • End date
    Aug 24, 2028
  • participants needed
  • sponsor
    QuesGen Systems Inc
Updated on 5 March 2022


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.

Condition Arrhythmia
Clinical Study IdentifierNCT03604133
SponsorQuesGen Systems Inc
Last Modified on5 March 2022


Yes No Not Sure

Inclusion Criteria

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

Exclusion Criteria

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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