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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04904731
Other study ID # 3658/20
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 19, 2021
Est. completion date May 24, 2021

Study information

Verified date May 2021
Source Azienda Ospedaliera di Perugia
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The present investigation aims to assess the diaphragmatic thickening fraction, reflecting the diaphragmatic activity, during supine (baseline) and at 1 hour following prone position in patients assisted through non invasive ventilation due to hypoxemic acute respiratory failure related to COVID-19. Also, the impact of lung aeration and comfort were ascertained in the same setting


Description:

Primary aim is to asses the effects of body position on diaphragmatic thickening fraction (primary aim) and lung aeration and vital sign (secondary aims) in patents assisted via noninvasive ventilation (NIV) for hypoxemic acute respiratory failure (hARF) associated to COVID-19. All adult patients, admitted for hARF due to COVID-19 and requiring NIV were enrolled. Diaphragmatic thickening fraction, lung aeration assessed through ultrasound, comfort, and grade of sedation-agitation as well as vital signs, i.e., peripheral oxygen saturation, blood pressure, and breathing pattern were monitored during noninvasive ventilation in supine and after 1 hour following the switch to prone position.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date May 24, 2021
Est. primary completion date May 12, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - COVID-19 infection, - Age > 18 years, - NIV application, - ICU admission Exclusion Criteria: - Pregnancy, - All the conditions contraindicating prone position and NIV

Study Design


Intervention

Other:
Prone position
Patients were assisted in NIV in supine position that was switched in prone position for clinical purpouse

Locations

Country Name City State
Italy Gianmaria Cammarota Perugia Umbria

Sponsors (1)

Lead Sponsor Collaborator
Azienda Ospedaliera di Perugia

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diaphragmatic thickening fraction The fraction of diaphragmatic thickness variations during respiratory cycle At baseline, in supine position
Primary Diaphragmatic thickening fraction The fraction of diaphragmatic thickness variations during respiratory cycle After 1 hour following prone position application
Secondary Lung aeration Lung aeration assessed through sonography At baseline, in supine position
Secondary Peripheral oxygen saturation Reflects the grade of peripheral oxygenation At baseline, in supine position
Secondary Lung aeration Lung aeration assessed through sonography after 1 hour following prone position application
Secondary Peripheral oxygen saturation Reflects the grade of peripheral oxygenation after 1 hour following prone position application