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Clinical Trials/NCT03527992
NCT03527992
Recruiting
Not Applicable

Automated Oxygen Administration in Patients With Hypoxemic Pneumonia and Pleuropneumonia

University Hospital, Toulouse1 site in 1 country128 target enrollmentMarch 9, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pneumonia
Sponsor
University Hospital, Toulouse
Enrollment
128
Locations
1
Primary Endpoint
Length in days of hospital stay
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

Hypoxemic pneumonia is a major cause of hospitalization in Pulmonology. The patient's dependency on oxygen prevents early discharge from the hospital. An automated oxygen therapy is a system that allows administration of oxygen with a flow that is automatically adjusted to the patient's saturation, which is continuously monitored. This system has proven to be particularly effective with chronic obstructive pulmonary disease (COPD) patients, by decreasing the time spent in hypoxia and hyperoxia, and by accelerating the weaning of oxygen. Our hypothesis is that automated oxygen therapy leads to a diminution on the length of hospital stay.

Detailed Description

Prolonged hospitalization has many consequences, including loss of autonomy and nosocomial infection. Moreover, these complications themselves lead to an extension of the length of stay. This has an impact on the cost of care: several studies have shown that hospitalization is the most costly factor in the management of pneumonia, and that even a small amount of hospital stay, led to significant financial savings. Automated oxygen therapy is a device that automatically adjusts with the saturation the amount of oxygen administered. Investigator hypothesis is that automated oxygen therapy could shorten the length of stay of patients hospitalized for hypoxemic pneumonia. One group of patients will receive the automated oxygen therapy and the other group will receive the standard Oxygen therapy. The investigator will compare in each group the average length of stay, the duration of oxygen therapy, the time spent outside of the target saturation, the cost on the medical-economic level and the patient's experience.

Registry
clinicaltrials.gov
Start Date
March 9, 2018
End Date
October 2028
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient living at home or in an institution
  • Patient hospitalized for less than 48 hours
  • Pneumonia defined (according to the 2006 French-speaking infectious pneumology society (SPILF) criteria) by:
  • respiratory functional symptoms (cough, sputum, dyspnea, chest pain) and
  • Hyperthermia \>38,5°C or hypothermia \<36°C and
  • Radiological Signs of Pneumonia
  • Hypoxia : SpO2 \< 94% in ambient air and/or PaO2\< 60 mmHg in ambient air

Exclusion Criteria

  • Pneumonia acquired at the hospital.
  • Patient hospitalized in another department more than 48 hours before admission
  • Chronic respiratory failure
  • Active neoplasia
  • Patients undergoing oxygen therapy and / or long-term NIV
  • Associated cardiac decompensation (clinical signs and / or NTproBNP\> 1800ng / mL) (3
  • Initial Need for high flow oxygen therapy or ventilatory support (NIV, VI)
  • Difficulties expected from home support.

Outcomes

Primary Outcomes

Length in days of hospital stay

Time Frame: 1 month

measure of total days of hospitalization and intensive care

Secondary Outcomes

  • quality questionnaire of patient's life during hospitalization(1 month)
  • Time spent outside of the target saturation(1 month)
  • rate of medical complication(1 month)
  • Duration of oxygen therapy(1 month)
  • the cost on the medical-economic level(1 month)

Study Sites (1)

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