Clinical and Functional Outcomes of Critically Ill Patients With COVID-19

NCT05024500 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2023-03-07

No results posted yet for this study

Summary

People affected by Severe Acute Respiratory Syndrome (SARS) by COVID-19 virus my require a long lasting invasive mechanical ventilation life support. To prevent damages to the lungs a number of protective lung ventilation measures are taken, one of them encounters the positive end expiratory pressure (PEEP) titration. Up to date, it is unclear the best method to titrate PEEP considering this unconventional syndrome compared to other etiologies. In addition to the long lasting advanced life support and bedridden condition, other factors may affect respiratory and peripheral muscle function of these patients. Therefore, the investigators intend to follow up these patients randomized to one of the three-arm experimental PEEP titration and after ICU discharge their status on clinical, laboratory and physical functions assessments.

Conditions

  • Acute Respiratory Distress Syndrome (ARDS)

Interventions

OTHER

ARDSNet table

The setting of the lowest PEEP level and FiO2 match stated by the table to achieve a goal oxygenation.

OTHER

Driving Pressure

The setting of the lowest PEEP level by the lowest correspondent driving pressure, which is defined by the difference of plateau pressure, after a modified alveolar recruitment maneuver.

OTHER

Electrical Impedance Tomography

The setting of the PEEP level above the intersection of the curves representing relative alveolar overdistention and collapse, after a modified alveolar recruitment maneuver.

Sponsors & Collaborators

  • Universidade Federal de Pernambuco

    collaborator OTHER
  • Coordination for the Improvement of Higher Education Personnel

    collaborator OTHER
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico

    collaborator OTHER_GOV
  • Fundação de Amparo à Ciência e Tecnologia de Pernambuco

    collaborator OTHER
  • University of Pernambuco

    lead OTHER

Principal Investigators

  • Shirley Lima Campos, PhD · Universidade Federal de Pernambuco

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-10-21
Primary Completion
2021-07-11
Completion
2022-12-30

Countries

  • Brazil

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05024500 on ClinicalTrials.gov