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Comparison of Oxygen Delivery Devices for Reversal of Altitude-Induced Hypoxemia in Normal Subjects

NCT01477450 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2014-09-26

Study results available
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Summary

This study will compare the ability of pulsed-dose oxygen from a concentrator to reverse altitude-induced hypoxemia compared to compressed gas from a standard oxygen cylinder.

Conditions

  • Hypoxemia
  • Hypobaric Hypoxemia

Interventions

DEVICE

Pulse-dose oxygen

Pulsed-dose oxygen delivery from an oxygen concentrator

DEVICE

Cylinder oxygen delivery

Oxygen delivery from an oxygen cylinder

Sponsors & Collaborators

  • United States Air Force

    collaborator FED

  • University of Cincinnati

    lead OTHER

Principal Investigators

  • Richard Branson, MSc RRT · University of Cincinnati

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-10-31
Primary Completion
2012-03-31
Completion
2012-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01477450 on ClinicalTrials.gov