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NCT01302470 · ClinicalTrials.gov registry record · NA

Comparison of Epicardial Versus Conventional Lead Placement in Cardiac Resynchronization Therapy

A NA study, sponsored by St. Luke's-Roosevelt Hospital Center.

Completed
Registry status
NA
Development phase
30
Enrollment target

NCT01302470 is a NA study that has completed, run by St. Luke's-Roosevelt Hospital Center. The registered enrollment target is 30 participants.

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The verdict

NCT01302470, a NA study, has completed, sponsored by St. Luke's-Roosevelt Hospital Center.

COMPLETED
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

The primary goal of this study is to evaluate the use of robotically -assisted device leads as a primary strategy for heart resynchronization.This trials aims to compare transvenous lead placement with robotic lead placement for cardiac resynchronization therapy.

Interventions

  • PROCEDURE Primary epicardial placement of left ventricular lead
  • PROCEDURE Transvenous placement of left ventricular lead

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2005-02
Est. Completion 2012-03
Phase NA

What the Registry Record Tells You About NCT01302470

The ClinicalTrials.gov registry entry for NCT01302470 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is St. Luke's-Roosevelt Hospital Center, which has 57 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Primary epicardial placement of left ventricular lead is the first listed.

NCT01302470 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01302470 about?

NCT01302470 is a clinical study titled "Comparison of Epicardial Versus Conventional Lead Placement in Cardiac Resynchronization Therapy". The primary goal of this study is to evaluate the use of robotically -assisted device leads as a primary strategy for heart resynchronization.This trials aims to compare transvenous lead placement with robotic lead placement for cardiac resynchronization therapy.

What is the current status of trial NCT01302470?

This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2005-02. Estimated completion is 2012-03.

What interventions are being tested in trial NCT01302470?

The interventions under investigation include: Primary epicardial placement of left ventricular lead (PROCEDURE), Transvenous placement of left ventricular lead (PROCEDURE).

Who is sponsoring clinical trial NCT01302470?

This trial is sponsored by St. Luke's-Roosevelt Hospital Center, which has 57 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.