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NCT Number: NCT01705119

The Effects of Vertical Position on Gas Exchange in Patients With Respiratory Failure

The purpose of this study is to investigate how changing from a supine to upright position affects gas exchange for patients with hypoxemic respiratory failure.

The research question is: will oxygen saturation and/or partial pressure of oxygen in the blood change when a patient with hypoxemic respiratory failure moves from a supine to upright position?

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This study is active but is not currently recruiting participants.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Chicago Medical Center

Chicago, Illinois, 60637, United States

About this study

Our hypothesis is that blood oxygen tension will not decrease and may even increase when a patient with respiratory failure stands up. Supine positioning often causes partial lung collapse, which results in a decreased amount of lung being available for gas exchange. In patients with Acute Respiratory Distress Syndrome (ARDS), tilting the patient up in bed has been shown to increase oxygen tension and improve lung compliance. Positional changes are sometimes used as a "rescue" intervention in patients with severe hypoxemia from ARDS. The investigators hope to conclude that severe hypoxemia should not be viewed as a contraindication to physical therapy, but rather physical therapy may be a potential intervention for patients with marginal gas exchange.

After sedative interruption, physical therapists and nursing staff will assist mechanically ventilated patients in moving to the side of the bed. They will assess the extremity strength using the MRC scale. If lower extremity strength is at least 4/5, the patient will be assisted to assume the upright position. The investigators will monitor the patient continuously and the session will be stopped at any point for

A. Mean arterial pressure <65 B. Heart rate <40, >130 beats/min C. Respiratory rate <5, >40 breaths/ min D. Pulse oximetry <88% E. Marked ventilator dyssynchrony F. Patient distress G. New arrhythmia H. Concern for myocardial ischemia I. Concern for airway device integrity J. Endotracheal tube removal

At this point, the patient's vital signs, pulse oximetry, and measures of lung compliance will be obtained. If an arterial line is in place and there have been ventilator adjustments since the morning arterial blood gas, the investigators will draw an arterial blood gas.

The physical therapists and nursing staff will then help the patient stand up. After one minute, the investigators will record another set of vital signs, pulse oximetry, and measures of lung compliance from the mechanical ventilator. If an arterial line is in place, the investigators will draw another arterial blood gas.

The patient will then be assisted back into bed. One hour later, the investigators will record the patient's vital signs, pulse oximetry, and measures of lung compliance from the mechanical ventilator.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged ≥18 years who are mechanically ventilated
  • An oxygen saturation of 88-94% or an arterial line

Exclusion criteria

  • Mean arterial pressure <65
  • Heart rate < 40 or > 130 beats/min
  • Respiratory rate < 5 or > 40 breaths/min
  • Pulse oximetry < 88%
  • Evidence of elevated intracranial pressure
  • Active gastrointestinal blood loss
  • Active myocardial ischemia
  • Pregnancy
  • Actively undergoing a procedure
  • Patient agitation requiring increased sedative administration in the last 30 mins
  • Insecure airway (device)
  • The patient was not ambulatory prior to hospitalization
  • The patient's body habitus and/or mental status make it unsafe to stand up
  • The patient has been placed on strict bed rest by the treating physicians

Treatment and study plan

Standing

Other

Primary outcomes

  1. PaO2 to FiO2 ratio

    Time frame: change from baseline to 1 hr

Secondary outcomes

  1. Oxygen Saturation

    Time frame: change from baseline to 1 hr

  2. change in blood PCO2

    Time frame: change from baseline to 1 hr

  3. Change in blood pH

    Time frame: change from baseline to 1hr

Other outcomes

  1. Tidal Volume

    Time frame: change from baseline to 1 hr

  2. Vital Signs

    Time frame: change from baseline to 1hr

Sponsors and collaborators

Lead sponsor

University of Chicago

Other

Registry information

Important dates

Study start
2012
Primary completion
2021
Study completion
2026
First posted
Oct 12, 2012
Registry last updated
Jan 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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