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NCT00632372 · ClinicalTrials.gov registry record

Cardiac Resynchronization Therapy (CRT) Based Heart Failure Monitoring Study

A clinical trial, sponsored by Abbott Medical Devices.

Completed
Registry status
8
Enrollment target

NCT00632372: Completed study, sponsored by Abbott Medical Devices.

NCT00632372 is a clinical trial that has completed, run by Abbott Medical Devices. The registered enrollment target is 8 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00632372 has completed, sponsored by Abbott Medical Devices.

COMPLETED
Registry status
8 participants
Enrollment target

Study Summary

The purpose of this study is to collect and analyze electrical measurements, timing, and signals from a CRT-D device in heart failure patients who either already have an implanted left atrial pressure sensor or will undergo a simultaneous implantation of a left atrial pressure sensor and a CRT-D device. These devices may be placed at the same time or separately (staged procedure) at the discretion of the investigator. A comparison will be made between the information gathered from the CRT-D system and the information gathered by the left atrial pressure sensor.

Interventions

  • DEVICE Cardiac Resynchronization Therapy
  • DEVICE HeartPOD™ System

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2008-01
Est. Completion 2015-12
Abbott Medical Devices

261 total trials

What the finished NCT00632372 record still lists

NCT00632372 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 8 participants, a relatively small participant target.

The record links to 0 conditions, and to 2 interventions - of which Cardiac Resynchronization Therapy is the first listed.

NCT00632372 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00632372 about?

NCT00632372 is a clinical study titled "Cardiac Resynchronization Therapy (CRT) Based Heart Failure Monitoring Study". The purpose of this study is to collect and analyze electrical measurements, timing, and signals from a CRT-D device in heart failure patients who either already have an implanted left atrial pressure sensor or will undergo a simultaneous implantation of a left atrial pressure sensor and a CRT-D dev...

What is the current status of trial NCT00632372?

This trial is currently completed. The enrollment target is 8 participants. The study started on 2008-01. Estimated completion is 2015-12.

What interventions are being tested in trial NCT00632372?

The interventions under investigation include: Cardiac Resynchronization Therapy (DEVICE), HeartPOD™ System (DEVICE).

Who is sponsoring clinical trial NCT00632372?

This trial is sponsored by Abbott Medical Devices, which has 261 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT00632372, the US trial registry maintained by the National Library of Medicine. NCT00632372 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.