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Filters: Condition: Device Advisory Clear all

Completed No phase listed Observational Results available

REPLACE: Implantable Cardiac Pulse Generator Replacement Registry

NCT00395447

View directory record Official record

Conditions: Device Replacement, Elective Replacement (ERI), Device Advisory, Device Upgrade, Postoperative Complications
Interventions: Straight-forward Device Replacement, Device Replacement with Upgrade; Procedure
Lead sponsor: Biotronik, Inc.; Industry
Eligibility: 18 Years and older

Enrollment: 1,744 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2007 – 2009
U.S. locations: 71
States / cities: Birmingham, Alabama • Mesa, Arizona • Modesto, California + 58 more

Source: ClinicalTrials.gov public record

Updated Apr 13, 2015 · Synced May 22, 2026, 1:05 AM EDT