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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04694638
Other study ID # 20-003191
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 21, 2020
Est. completion date May 10, 2023

Study information

Verified date October 2023
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This research aims to understand if prone positioning combined with high-flow nasal cannula (HFNC) or non-invasive positive pressure ventilation (NIPPV) safely reduce the rate of intubation in acute hypoxemic and/or hypercapnic respiratory failure secondary to COVID-19 infection.


Recruitment information / eligibility

Status Completed
Enrollment 6
Est. completion date May 10, 2023
Est. primary completion date May 10, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 110 Years
Eligibility Inclusion Criteria: - Patients with confirmed COVID19 infection or suspected COVID19 infection. - Patients requiring HFNC or NIPPV - Patients who are clinically stable and able to tolerate the changes in position that are routinely conducted as part of the standard of care in the medical ICU. - Patient should be able to provide informed consent to the study. Any participant speaking any language will be offered participation. - Able to actively participate in Assisted Manual Pronation Therapy per nursing assessment. Exclusion Criteria: Contraindication for prone positioning: - Intracranial pressure >30 mm Hg or cerebral perfusion pressure <60 mmHg - Massive hemoptysis requiring an immediate surgical or interventional radiology procedure - Tracheal surgery or sternotomy during the previous 15 days - Serious facial trauma or facial surgery during the previous 15 days - Deep venous thrombosis treated for less than 2 days - Cardiac pacemaker inserted in the last 2 days - Unstable spine, femur, or pelvic fractures - Hemodynamic instability or severe cardiac arrhythmia (chronic AFib is not a contraindication). Mean arterial pressure lower than 60 mm Hg, >1 vasopressor agent or Norepinephrine equivalent dose >0.06 mcg/kg/min - Pregnant women - Single anterior chest tube with air leaks - Burns on more than 20 % of the body surface - Delirium or altered mental status increasing fall risk while in prone position. - End-of-life decision before inclusion - Subject deprived of freedom, minor, subject under a legal protective measure - Unable to actively participate in Assisted Manual Pronation Therapy per nursing assessment - Lacking capacity to provide informed consent. - Individuals with mechanical or vascular disease precluding safe displacement of the head, for example: cervical spinal fusion, limited range of motion, or severe vascular occlusive disease of the head and neck. - Body mass index (BMI) greater than 70 kg/m2, or unable to actively participate in Assisted Manual Pronation Therapy per nursing assessment at any BMI value.

Study Design


Intervention

Other:
Body position change
combined use of prone positioning and high-flow nasal cannula (HFNC) and non-invasive positive pressure ventilation (NIPPV) can reduce the rate of intubation in acute hypoxemic and/or hypercapnic respiratory failure secondary to COVID-19 infection.

Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of intubation Number of critically ill patients with acute hypoxemic and/or hypercapnic respiratory failure, secondary to COVID-19 infection to require intubation and mechanical ventilation 1 year
Secondary Incidence of hypotension and cardiac arrhythmias and other nursing-related risks of combining prone positioning with high-flow nasal cannula and non-invasive positive pressure ventilation To evaluate the the incidence of hypotension and cardiac arrhythmias and other nursing-related risks of combining prone positioning with high-flow nasal cannula and non-invasive positive pressure ventilation. 1 year
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