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NCT01214200 · ClinicalTrials.gov registry record · NA

High Intensity Non-Invasive Positive Pressure Ventilation (HINPPV)

A NA study, sponsored by Philips Respironics.

Completed
Registry status
NA
Development phase
20
Enrollment target

NCT01214200 is a NA study that has completed, run by Philips Respironics. The registered enrollment target is 20 participants.

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The verdict

NCT01214200, a NA study, has completed, sponsored by Philips Respironics.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target

Study Summary

The purpose of this pilot study is to evaluate the effect of high intensity non-invasive positive pressure ventilation (HINPPV) for stable, hypercapnic COPD patients. The investigators believe that HINPPV, used at least 6 hours nocturnally over three months, will benefit the stable hypercapnic COPD patient through a reduction in the daytime partial pressure of carbon dioxide in arterial blood (PaCO2) levels.

Interventions

  • DEVICE Bilevel positive airway pressure (BiPAP)

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2010-08
Est. Completion 2012-12
Phase NA

Sponsor

Philips Respironics

35 total trials

What the Registry Record Tells You About NCT01214200

The ClinicalTrials.gov registry entry for NCT01214200 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Philips Respironics, which has 35 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Bilevel positive airway pressure (BiPAP) is the first listed.

NCT01214200 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01214200 about?

NCT01214200 is a clinical study titled "High Intensity Non-Invasive Positive Pressure Ventilation (HINPPV)". The purpose of this pilot study is to evaluate the effect of high intensity non-invasive positive pressure ventilation (HINPPV) for stable, hypercapnic COPD patients. The investigators believe that HINPPV, used at least 6 hours nocturnally over three months, will benefit the stable hypercapnic COPD ...

What is the current status of trial NCT01214200?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2010-08. Estimated completion is 2012-12.

What interventions are being tested in trial NCT01214200?

The interventions under investigation include: Bilevel positive airway pressure (BiPAP) (DEVICE).

Who is sponsoring clinical trial NCT01214200?

This trial is sponsored by Philips Respironics, which has 35 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.