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NCT01555619: Quad PAS

Quadripolar Pacing Post Approval Study

Completed Last updated 16 April 2019
What this trial tests

trial testing CRT-D System in Heart Failure in 1,971 participants. Completed in 28 February 2019.

Timeline
15 February 2012
Primary endpoint
28 February 2019
28 February 2019

Quick facts

Lead sponsorAbbott Medical Devices
StatusCompleted
Study typeOBSERVATIONAL
Enrollment1,971
Start date15 February 2012
Primary completion28 February 2019
Estimated completion28 February 2019
Sites71 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Abbott Medical Devices — full company profile →

Who can join

18 and older, any sex, with Heart Failure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this post-approval study is to evaluate the acute and chronic performance of a Quadripolar CRT-D device system in a patient population indicated for cardiac resynchronization therapy (CRT).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Performance of the quadripolar CRT-D system: Five-year results from the Quadripolar Pacing Post-Approval Study.
    Corbisiero R, Cao M, Muller D, Lee K, et al · · 2025 · PMID 38971416 · DOI 10.1016/j.hrthm.2024.07.006

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Other recruiting trials for Heart Failure

Currently open trials in the same condition.

Other Abbott Medical Devices trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01555619.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing