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NCT03119727 | COMPLETED | Respiratory Disease


Clinical Evaluation of FreeO2 (Version 4) in All Patients Receiving Oxygen
Sponsor:

Laval University

Information provided by (Responsible Party):

François Lellouche

Brief Summary:

Evaluation of automatic titration of oxygen with a new version of FreeO2 (V4)

Condition or disease

Respiratory Disease

Respiratory Failure

COPD Exacerbation

Asthma

Pneumonia

Intervention/treatment

FreeO2

Phase

NA

Detailed Description:

In the previous studies, the investigators used many times automatic titration of oxygen on spontanous breathing patient (FreeO2 device) with a prototype develop in our lab in collaboration with Laval university. In this study, we want to evaluate the new version of the FreeO2 device (V4)

Study Type : INTERVENTIONAL
Estimated Enrollment : 50 participants
Masking : NONE
Primary Purpose : OTHER
Official Title : Clinical Evaluation of the Automatic Oxygen Adjustment by FreeO2 in a Medical Population in Hospital
Actual Study Start Date : 2017-01-30
Estimated Primary Completion Date : 2019-04-30
Estimated Study Completion Date : 2020-11-06

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • * Age \> or = 18 years old
  • * Patient receiving oxygen between 1 to 6 lpm for medical pathology
  • * Admitted to a medical service for less than 72 hours (emergency room not included)
Exclusion Criteria
  • * Unreliable SpO2 signal
  • * Emergency or intensive care hospitalization
  • * Absence of NIV or intubation criteria at baseline
  • * Sleep apnea not paired
  • * Long-term Oxygen Therapy
  • * Active delirium and cognitive impairment preventing informed consent

Clinical Evaluation of FreeO2 (Version 4) in All Patients Receiving Oxygen

Location Details

NCT03119727


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Locations


Not yet recruiting

Canada,

IUCPQ-UL

Quebec, Canada, G1V4G5

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