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NCT00484562 · ClinicalTrials.gov registry record · NA
Prospective Study Comparing Different Modalities of Oxygen Delivery During Assessment of Functional Exercise Capacity
A NA study, sponsored by University of Missouri-Columbia.
- Completed
- Registry status
- NA
- Development phase
- 39
- Enrollment target
NCT00484562 is a NA study that has completed, run by University of Missouri-Columbia. The registered enrollment target is 39 participants.
The verdict
NCT00484562, a NA study, has completed, sponsored by University of Missouri-Columbia.
- COMPLETED
- Registry status
- NA
- Development phase
- 39 participants
- Enrollment target
Study Summary
Objectives: The objective of this study is to determine if any differences exist between the varying modes of portable oxygen delivery systems including liquid oxygen, a portable concentrator, portable devices filled at home from a concentrator, and medical grade compressed oxygen (either an M6 size or D size cylinder). Hypothesis: Patients who are prescribed LTOT will show similar physiologic responses to exercise when using differing modalities of portable oxygen delivery systems.
Interventions
- DEVICE Standard oxygen delivery system
- DEVICE Homefill oxygen delivery system
- DEVICE Helios oxygen delivery system
- DEVICE FreeStyle oxygen system
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 39 participants |
| Start Date | 2006-05 |
| Est. Completion | 2006-09 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00484562
The ClinicalTrials.gov registry entry for NCT00484562 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 39 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Missouri-Columbia, which has 291 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 4 interventions - of which Standard oxygen delivery system is the first listed.
NCT00484562 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00484562 about?
NCT00484562 is a clinical study titled "Prospective Study Comparing Different Modalities of Oxygen Delivery During Assessment of Functional Exercise Capacity". Objectives: The objective of this study is to determine if any differences exist between the varying modes of portable oxygen delivery systems including liquid oxygen, a portable concentrator, portable devices filled at home from a concentrator, and medical grade compressed oxygen (either an M6 siz...
What is the current status of trial NCT00484562?
This trial is currently completed. It is a NA study. The enrollment target is 39 participants. The study started on 2006-05. Estimated completion is 2006-09.
What interventions are being tested in trial NCT00484562?
The interventions under investigation include: Standard oxygen delivery system (DEVICE), Homefill oxygen delivery system (DEVICE), Helios oxygen delivery system (DEVICE), FreeStyle oxygen system (DEVICE).
Who is sponsoring clinical trial NCT00484562?
This trial is sponsored by University of Missouri-Columbia, which has 291 total clinical trials registered on ClinicalTrials.gov.
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