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Elective Replacement (ERI) clinical trials

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NCT ID: NCT00395447 Completed - Clinical trials for Postoperative Complications

REPLACE: Implantable Cardiac Pulse Generator Replacement Registry

REPLACE
Start date: July 2007
Phase: Phase 4
Study type: Observational

The objective of this study is to prospectively estimate the all-cause complication rates at 6-months for patients undergoing generator replacement due to elective replacement indicator (ERI), advisory, or upgrade without a planned system modification or with a planned system modification. Secondarily, this study aims to compare the influence of baseline variables contributing to the all-cause complication rates for subjects undergoing generator replacement.