An Observational Study of Non-Invasive Respiratory Volume Monitoring After Extubation of Surgical and Neurological Patients Admitted to the Intensive Care Unit
Overview
Tab Title Description
Study type
ObservationalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Jacksonville, Florida: 18-006035
Sponsor Protocol Number: 18-006035
About this study
The purpose of this study is to investigate the association of decreased minute ventilation and greater incidence of oxygen arterial desaturation, hypercapneic or hypoxemic respiratory failure that requires high flow nasal oxygen therapy, non-invasive ventilation or re-intubation following cardiothoracic surgical procedures.
Participation eligibility
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Inclusion Criteria:
- Patients aged 18-85 years of age, regardless of gender, ethnicity or background.
- Patient’s weight > 80 lbs who are intubated, with planned extubation and informed consent has been obtained previously.
- All patients who undergo cardiothoracic, vascular, neurosurgical and general, surgical procedures and receive ventilator mechanical support in the intensive care unit.
- All patients diagnosed with subarachnoid hemorrhage and stroke (hemorrhagic or ischemic) that require ventilator mechanical support in the intensive care unit.
Exclusion Criteria:
- Patient unable to give informed consent.
- Any patient whose condition will not allow for placement of the electrode PadSet.
- Left-side single lung transplantation. (Monitoring pads placed on right side of chest would be over diseased lung and inaccurate) .
Participating Mayo Clinic locations
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
| Mayo Clinic Location |
Status |
|
Jacksonville, Fla.
Mayo Clinic principal investigator John Moss, M.D. |
Closed for enrollment |
|
More information
Publications
Publications are currently not available