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Non-Invasive Ventilation After Extubation in Hypercapnic Patients

Non-Invasive Ventilation After Extubation in Hypercapnic Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00539708
Enrollment
106
Registered
2007-10-04
Start date
2005-05-31
Completion date
2008-04-30
Last updated
2008-05-12

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

Conditions

Respiratory Failure

Keywords

Non-invasive ventilation, Hypercapnic respiratory failure, Mechanical ventilation, Respiratory failure after extubation

Brief summary

The purpose of this study is to assess the efficacy of noninvasive ventilation in the prevention of extubation failure and mortality in patients with chronic respiratory disorders and hypercapnic respiratory failure during spontaneous breathing.

Detailed description

Background and aims: Patients with chronic respiratory disorders, intubated and mechanically-ventilated in intensive care units (ICU), often exhibit hypercapnia during the spontaneous breathing trial prior to extubation; this is associated to increased incidence of extubation failure and mortality. We will assess the efficacy of noninvasive ventilation (NIV) in the prevention of extubation failure and mortality in these patients. Design: Prospective, randomized, controlled clinical trial with two groups: support with noninvasive ventilation, and conventional clinical management (control group). Subjects: Patients with chronic respiratory disorders, intubated and ventilated ³48 hours, with hypercapnia (PaCO2 \>45 mmHg) during the spontaneous breathing trial, ready to be extubated. Interventions: Random allocation into two groups: NIV immediately after extubation during 24 hours, on conventional clinical management. Clinical follow-up (incidence of extubation failure, reintubation, ICU and hospital mortality, 90-day survival, complications associated to mechanical ventilation, ICU and hospital length of stay). Analyses of data: Comparison between two groups (NIV and control) in non-paired data design: quantitative variables (t-test, Mann-Whitney test, ROC curves), qualitative or categorical variables (chi square, Fisher's exact test), and Kaplan-Meier estimate of survival curves).

Interventions

PROCEDURENon-invasive ventilation

Non-invasive ventilation after extubation for 24 hours

Sponsors

Fondo de Investigacion Sanitaria
CollaboratorOTHER
Hospital Clinic of Barcelona
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Chronic respiratory disorders with invasive mechanical ventilation * Hypercapnic respiratory failure during successful spontaneous breathing trial

Exclusion criteria

* Face or cranial trauma or surgery * Recent gastric or esophageal surgery * Tracheostomy or other upper airway disorders * Upper gastrointestinal bleeding * Excess respiratory secretions * Lack of collaboration

Design outcomes

Primary

MeasureTime frame
Primary outcome: The incidence of respiratory failure after extubation3 days after extubation

Secondary

MeasureTime frame
Survival90 days

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026