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NCT00288587 · ClinicalTrials.gov registry record · Phase 4

Extracorporeal Ultrafiltration (UF) vs. Usual and Customary Care for Patients With Severe Heart Failure (HF)

A Phase 4 study of Heart Failure and CHF, sponsored by NxStage Medical.

Completed
Registry status
Phase 4
Development phase
36
Enrollment target
1
Study location

NCT00288587 is a Phase 4 study of Heart Failure and CHF that has completed, run by NxStage Medical. The registered enrollment target is 36 participants, below the 2,049-participant average among 397 other Heart Failure trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00288587, a Phase 4 study of Heart Failure and CHF, has completed, sponsored by NxStage Medical.

COMPLETED
Registry status
Phase 4
Development phase
36 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to assess the ability of Ultrafiltration to influence the rate of hemodynamic improvement, as measured by the decline in the pulmonary artery occlusion pressure, in patients with NYHA class III/IV Heart Failure.

Conditions Studied

Interventions

  • DEVICE NxStage System One
  • DRUG IV loop diuretic

Study Locations (1)

Ohio

  • The Cleveland Clinic Foundation - Cleveland

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2003-10
Est. Completion 2009-01
Phase Phase 4

Sponsor

NxStage Medical

3 total trials

What the Registry Record Tells You About NCT00288587

The ClinicalTrials.gov registry entry for NCT00288587 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,049-participant average among 397 other Heart Failure trials with a reported enrollment target (98% lower). The listed sponsor is NxStage Medical, which has 3 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Heart Failure appearing as the primary indexed condition, and to 2 interventions - of which NxStage System One is the first listed.

NCT00288587 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT00288587 about?

NCT00288587 is a clinical study titled "Extracorporeal Ultrafiltration (UF) vs. Usual and Customary Care for Patients With Severe Heart Failure (HF)". The purpose of this study is to assess the ability of Ultrafiltration to influence the rate of hemodynamic improvement, as measured by the decline in the pulmonary artery occlusion pressure, in patients with NYHA class III/IV Heart Failure.

What is the current status of trial NCT00288587?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 36 participants. The study started on 2003-10. Estimated completion is 2009-01.

What conditions does trial NCT00288587 study?

This clinical trial studies the following conditions: Heart Failure, CHF.

What interventions are being tested in trial NCT00288587?

The interventions under investigation include: NxStage System One (DEVICE), IV loop diuretic (DRUG).

Who is sponsoring clinical trial NCT00288587?

This trial is sponsored by NxStage Medical, which has 3 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00288587 being conducted?

This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.