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Clinical Trials in China / NCT06014034
Active, not recruiting Not applicable

Randomized Controlled Study of Programmed Weaning From NIV for AECOPD

NCT06014034 · tracked via the Priya Life Science China tracker
Sponsor
Peking University Third Hospital
Phase
Not applicable
Started
2023-05-12
Last updated
2026-06-11

Condition(s) studied

Acute Exacerbation of COPD

Investigational drug(s) / intervention(s)

Programmed Weaning From Noninvasive Mechanical Ventilation

Programmed Weaning From Noninvasive Mechanical Ventilation: Programmed withdrawal unit: daily morning review arterial blood gas analysis (since the 2nd, daily morning stop non-invasive ventilation 1 hours, 2 hours, 3 hours, 4 hours after check arterial blood gas analysis), blood gas results suggest respiratory acidosis compensatory period (pH value greater than 7.35) can reduce daily noninvasive ventilation time, namely the noninvasive ventilation use time for 24 hours, 20 hours, the third day 16 hours, the fourth 12 hours, fifth day 8 hours. If ABG indicates still acid decompensation, continue the non-invasive ventilation regimen of the previous day. If noninvasive ventilation failed, invasive mechanical ventilation was performed.

Study summary

Purpose of research:to explore a reasonable programmed withdrawal process of noninvasive ventilation and thereby reduce the duration of noninvasive mechanical ventilation in patients with acute exacerbations of chronic obstructive pulmonary disease.

Eligibility

Sex
ALL
Min age
40 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * It is defined that in patients with acute exacerbation of chronic obstructive pulmonary disease, the arterial blood gas analysis was decompensation of respiratory acidosis, and the pH value was 7.20-7.35 * Non-invasive mechanical ventilation was performed and it was well tolerated Exclusion Criteria: * younger than 40 years old * pregnancy * Human immunodeficiency virus (HIV) antibody was positive * Hemodynamic instability * Long-term use of home non-invasive ventilators * Mechanical ventilation for endotracheal intubation and cardiopulmonary resuscitation were disagreed

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Peking University Third Hospita Beijing Beijing Municipality

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06014034 on ClinicalTrials.gov ↗ ← All trials in China