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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: Completed NA study, sponsored by Philips Respironics.
NCT01214200 is a NA study that has completed, run by Philips Respironics. The registered enrollment target is 20 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Daytime PaCO2 levels assessed after using high intensity non-invasive positive pressure ventilation (HINPPV) are compared to the participants' baseline daytime PaCO2 levels.
Interventions
- DEVICE Bilevel positive airway pressure (BiPAP)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2010-08 |
| Est. Completion | 2012-12 |
| Phase | NA |
What the finished NCT01214200 record still lists
NCT01214200 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which Bilevel positive airway pressure (BiPAP) is the first listed.
NCT01214200 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01214200's enrollment target sits among peer trials
20 1768th of 2000 higher than 140 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
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