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COMPLETED

Quadripolar Pacing Post Approval Study

NCT01555619 · View on ClinicalTrials.gov ↗

Study Summary

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).

Conditions Studied

Interventions

  • DEVICE CRT-D System

Study Locations (20)

California

  • Comprehensive Cardiovascular — Bakersfield
  • Scripps Green Hospital — La Jolla
  • USC Unversity Hospital — Los Angeles
  • Fogarty Institute — Mountain View
  • Premier Cardiology, Inc. — Newport Beach
  • Cardiac Rhythm Specialists, Inc. — Northridge
  • St. Joseph Heritage Medical Group — Orange
  • Regional Cardiology Associates — Sacramento
  • St. Joseph's Medical Center — Stockton
  • Cardiology Associates Medical Group, Inc. — Ventura

Florida

  • Florida Electrophysiology Associates — Atlantis
  • Yoel R. Vivas, MD — Boynton Beach
  • Jorge Diaz — Lake Mary
  • Naples Heart Rhythm Specialists — Naples

Alabama

  • Cardiology, P.C. — Birmingham
  • Heart Center Research, LLC/Research Center — Huntsville
  • Southeastern Cardiology Consultants PC — Montgomery

Arkansas

  • Washington Regional Medical Center — Fayetteville
  • Arkansas Heart Hospital — Little Rock

Arizona

  • Arizona Arrhythmia Research Center — Phoenix

Trial Details

FieldValue
Enrollment Target 1,971 participants
Start Date 2012-02-15
Est. Completion 2019-02-28

Sponsor

Abbott Medical Devices

155 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01555619

The ClinicalTrials.gov registry entry for NCT01555619 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,971 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abbott Medical Devices, which has 155 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Heart Failure appearing as the primary indexed condition, and to 1 intervention — of which CRT-D System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01555619 reports 20 study locations spanning 5 distinct geographic areas — top geographies include California, Florida, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01555619 about?

NCT01555619 is a clinical study titled "Quadripolar Pacing Post Approval Study". 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).

What is the current status of trial NCT01555619?

This trial is currently completed. The enrollment target is 1,971 participants. The study started on 2012-02-15. Estimated completion is 2019-02-28.

What conditions does trial NCT01555619 study?

This clinical trial studies the following conditions: Heart Failure. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01555619?

The interventions under investigation include: CRT-D System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01555619?

This trial is sponsored by Abbott Medical Devices, which has 155 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01555619 being conducted?

This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial