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Ambulatory Surgical Center Implantable Cardioverter-Defibrillator Outcomes Registry

Who can join

All ages · All sexes

Inclusion Criteria:

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

Exclusion Criteria:

* N/A

About the study

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.

Sponsor: QuesGen Systems Inc · Participants: 500 · Started: Aug 24, 2017

Contact the study team

• Michael Jarrett, MBA · Phone: 415-608-3570
• Martin Jorgensen, PhD · Phone: 650-777-7617

Official record on ClinicalTrials.gov — NCT03604133

Locations in the U.S.

Conditions

• Arrhythmia

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.