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NCT01520714 · ClinicalTrials.gov registry record · NA

Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds (EXPECT)

A NA study, sponsored by Baylor Research Institute.

Terminated
Registry status
NA
Development phase
11
Enrollment target

NCT01520714 is a NA study that was terminated before completion, run by Baylor Research Institute. The registered enrollment target is 11 participants.

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The verdict

NCT01520714, a NA study, was terminated before completion, sponsored by Baylor Research Institute.

TERMINATED
Registry status
NA
Development phase
11 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether changes in a patient's position affect LV capture thresholds in a clinically significant way.

Interventions

  • DEVICE Medtronic 4195 active fixation LV lead and Medtronic passive fixation LV lead

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2009-12
Est. Completion 2011-12
Phase NA

Sponsor

Baylor Research Institute

180 total trials

What the Registry Record Tells You About NCT01520714

The ClinicalTrials.gov registry entry for NCT01520714 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Baylor Research Institute, which has 180 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Medtronic 4195 active fixation LV lead and Medtronic passive fixation LV lead is the first listed.

NCT01520714 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01520714 about?

NCT01520714 is a clinical study titled "Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds (EXPECT)". The purpose of this study is to determine whether changes in a patient's position affect LV capture thresholds in a clinically significant way.

What is the current status of trial NCT01520714?

This trial is currently terminated. It is a NA study. The enrollment target is 11 participants. The study started on 2009-12. Estimated completion is 2011-12.

What interventions are being tested in trial NCT01520714?

The interventions under investigation include: Medtronic 4195 active fixation LV lead and Medtronic passive fixation LV lead (DEVICE).

Who is sponsoring clinical trial NCT01520714?

This trial is sponsored by Baylor Research Institute, which has 180 total clinical trials registered on ClinicalTrials.gov.

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

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.