Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00547729 · ClinicalTrials.gov registry record · NA

Hemodynamically Guided Home Self-Therapy in Severe Heart Failure Patients (HOMEOSTASIS)

A NA study, sponsored by Abbott Medical Devices.

Completed
Registry status
NA
Development phase
71
Enrollment target

NCT00547729: Completed NA study, sponsored by Abbott Medical Devices.

NCT00547729 is a NA study that has completed, run by Abbott Medical Devices. The registered enrollment target is 71 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00547729, a NA study, has completed, sponsored by Abbott Medical Devices.

COMPLETED
Registry status
NA
Development phase
71 participants
Enrollment target

Study Summary

This study is a feasibility study of the HeartPOD™ Heart Failure Management System with DynamicRx® (HeartPOD system) in patients with severe chronic congestive heart failure. The device being studied in this trial monitors heart function and alerts the patient and physician of necessary changes to medication. The study will assess the safety, reliability, and preliminary efficacy of the HeartPOD™ system.

Primary Outcome

Out of 71 subjects enrolled, data from 55 subjects was adjudicated by a Clinical Events Committee and included in this primary endpoint analysis. MACNE was defined as a hierarchical composite of cardiovascular related death, myocardial infarction, systemic thromboembolism and stroke.

Interventions

  • DEVICE HeartPOD™ System

Trial Details

FieldValue
Enrollment Target 71 participants
Start Date 2005-03
Est. Completion 2008-06
Phase NA
Abbott Medical Devices

261 total trials

What the finished NCT00547729 record still lists

NCT00547729 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 71 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 1 intervention - of which HeartPOD™ System is the first listed.

NCT00547729 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00547729 about?

NCT00547729 is a clinical study titled "Hemodynamically Guided Home Self-Therapy in Severe Heart Failure Patients (HOMEOSTASIS)". This study is a feasibility study of the HeartPOD™ Heart Failure Management System with DynamicRx® (HeartPOD system) in patients with severe chronic congestive heart failure. The device being studied in this trial monitors heart function and alerts the patient and physician of necessary changes to m...

What is the current status of trial NCT00547729?

This trial is currently completed. It is a NA study. The enrollment target is 71 participants. The study started on 2005-03. Estimated completion is 2008-06.

What interventions are being tested in trial NCT00547729?

The interventions under investigation include: HeartPOD™ System (DEVICE).

Who is sponsoring clinical trial NCT00547729?

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

How this trial's enrollment target compares

Where NCT00547729's enrollment target sits among peer trials

71 1102nd of 2000 higher than 898 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05452889 · 71 participants · Early Phase 1

    PET Image in PAH Patients

  • NCT05766943 · 71 participants · NA

    Reduction of Myopotential Interference With Smart Pass in S-ICD Patients

  • NCT06229678 · 71 participants · Early Phase 1

    Ketones, SGLT2, HFrEF

  • NCT06377566 · 71 participants · Phase 2

    A Study of BV-AVD in People With Bulky Hodgkin Lymphoma

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00547729, the US trial registry maintained by the National Library of Medicine. NCT00547729 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.