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The effect of returning the patient to the Resting Ventilator after performing the Spontaneous Breathing Test during the respirator withdrawal process

Efficacy of the Protocol of patient Reconnection to the Mechanical Ventilator after success in the Spontaneous Breathing Test for Ventilatory Weaning

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3x8nxn
Enrollment
Unknown
Registered
2019-06-14
Start date
2018-08-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiration, Artificial

Interventions

A checklist will be applied for patients eligible for teaching to assess the suitability for ventilatory weaning. Patients who are able to start the weaning process are called to perform the spontaneo
Other

Sponsors

Universidade da Região de Joinville - UNIVILLE
Lead Sponsor
Universidade da Região de Joinville - UNIVILLE
Collaborator
Hospital Municipal São José
Collaborator
Centro Hospitalar Unimed
Collaborator
Hospital Unimed Litoral
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age equal to or greater than 18 years; Patients intubated on mechanical ventilation for more than 12 hours;

Exclusion criteria

Exclusion criteria: Mechanical ventilation for more than 21 days; Patients with Glasgow Scale <8; Patients with no indication of cardiopulmonary resuscitation or reintubation; Formal indication of non-invasive ventilation after extubation due to hypercapnia during the spontaneous breathing test; Patients with spindle trauma, neuromuscular diseases. Failure to obtain the informed consent term or withdrawal of study participation at any time.

Design outcomes

Primary

MeasureTime frame
Evaluate the rate of tracheal reintubation within 48 hours after extubation has been performed. The percetual of reintubated patients will be verified in both the intervention group and the control group, and a comparison of the rates between groups will be performed.

Secondary

MeasureTime frame
Evaluate the length of hospital stay and ICU in days for the patients in the intervention and control group, and verify if there is a difference in the number of days between groups.;Evaluate the mortality rate during ICU and hospital stay in the patients in the intervention and control group, and verify if there is a difference in the number of days between groups.

Countries

Brazil

Contacts

Public ContactGlauco;Michelli Westphal;Dadam

Centro Hospitalar Unimed;Universidade da Região de Joinville - UNIVILLE

glauco.ww@gmail.com;mikidadam@gmail.com+55(47)999642295;+55(47)996138693

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 23, 2026