Early CPAP in COVID-19 Patients With Respiratory Failure.

Not Applicable

Completed

• Conditions: CPAP Ventilation; Emergency Departments; COVID-19
• Interventions: Device: CPAP treatment

• Registration Number: NCT04326075
• Lead Sponsor: Mario Negri Institute for Pharmacological Research

Brief Summary

The study aims at clarifying whether early treatment with continuous positive airway pressure (CPAP) ventilation is able to reduce the need for intubation or death in patients visiting an emergency department (ED) with known or suspected COVID-19 infection and insufficiency respiratory.

Detailed Description

Eligible patients will be randomized to two treatment arms: current clinical practice (control arm) and early treatment with CPAP in addition to current clinical practice (experimental arm). To deal with the current emergency situation, the study will adopt an adaptive design with a Bayesian continuous monitoring. Such design allows to stop the study as soon as the data provide sufficient evidence of efficacy or ineffectiveness of the studied treatment.

The primary endpoint of the study is the combination of intubation or death within 7 days of randomization. The secondary endpoint is 30-day mortality.

All patients arriving at the ED will be evaluated to verify the presence of inclusion and exclusion criteria. Randomization will be performed through an ad-hoc electronic case report form (eCRF). Eligible patients should be randomized as soon as possible, possibly immediately after the ED triage.

Patients randomized to the control arm will be treated according to current clinical practice, which currently does not involve the use of CPAP. Therefore, these patients should not start treatment with CPAP immediately after randomization. CPAP treatment, however, is allowed at a later stage, if deemed appropriate according to clinical judgment.

Patients randomized to the experimental arm should begin treatment with CPAP as soon as possible. CPAP should only be performed with a helmet, using a positive end-expiratory pressure (PEEP) between 8 and 14 cmH2O and an inspired oxygen fraction (FiO2) between 40 and 60%. FiO2 and PEEP must be modulated, within the limits indicated above, so as to obtain a saturation \> 94%. Whenever this goal cannot be achieved, the patient should be referred to the intensivist.

Study Timeline

• Study First Submitted: 2020-03-26
• Study First Submitted QC: 2020-03-27
• Study First Posted: 2020-03-30
• Study Start: 2020-12-01
• Primary Completion: 2021-06-30
• Status Verified: 2021-12
• Study Completion: 2022-12-15
• Last Update Submitted: 2022-12-16
• Last Update Posted: 2022-12-19

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 68

Inclusion Criteria

ED patients positive to or suspected of COVID-19 infection with at least one of the following symptoms:

• fever
• cough/dyspnea
• respiratory symptoms or ED arrival for respiratory reason and for whom there are the following conditions:
• SpO2 < 95% in ambient air or positive Quick Walk Test
• PaO2/FiO2 > 200 in ambient air or with Venturi mask, evaluated in 1 hour from ED arrival.

Exclusion Criteria

• BPCO patients
• Age > 70 years
• Pregnant status
• Contraindications for CPAP

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Early CPAP treatment	CPAP treatment	Early treatment with CPAP in addition to current clinical practice

Primary Outcome Measures

Name	Time	Method
Death or need of intubation	7 days since ED arrival	The study outcomes will be death or need of intubation within 7 days since ED arrival.

Secondary Outcome Measures

Name	Time	Method
30-day mortality	30 days since ED arrival	30-day mortality

Trial Locations

Locations (1)

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico; 🇮🇹 Milan, Italy