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Microcirculation in Spontaneous Breathing Trial

Association Between Change of Microcirculation After Spontaneous Breathing Trial and Ventilator Weaning

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04711590
Enrollment
59
Registered
2021-01-15
Start date
2019-12-05
Completion date
2022-09-30
Last updated
2022-12-14

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

Conditions

Critically Ill

Keywords

ventilator, weaning, microcirculation

Brief summary

Weaning ventilator support in critically ill patients is crucial. Both delayed extubation and unexpected early reintubation are harmful to the patients. Weaning parameters and spontaneous breathing trial are used to investigate the indication and predict the successful extubation. Hemodynamic stability and physical reserve are important indicators as well. Microcirculation parameters are known to be more sensitive to the change of hemodynamic status than macrocirculation parameters. We hypothesize that the change of sublingual microcirculation before and after spontaneous breathing trial is different between the the patients with successful extubation and the patients with failed extubation. Thus, this study measures sublingual microcirculation in patients receiving spontaneous breathing trial and record the extubation status (successful or failed). The microcirculation parameters before and after spontaneous breathing trial are compared between the the patients with successful extubation and the patients with failed extubation.

Interventions

Sublingual microcirculation images were recorded using an incident dark-field video microscope

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* critically ill patients received ventilator longer than 12 hours * ready for spontaneous breathing trial * GCS coma score equal or higher than 8

Exclusion criteria

* aged less than 20 years * patient with tracheostomy * patient and patients' relatives are non-native speakers

Design outcomes

Primary

MeasureTime frameDescription
Initial total vessel density0 hourTotal vessel density measured by Cytocam before and after spontaneous breathing trial
Change of total vessel densitybaseline and 1 hourThe difference between the total vessel density measure by Cytocam before and after spontaneous breathing trial

Secondary

MeasureTime frameDescription
Initial perfused vessel density0 hourPerfused vessel density measured by Cytocam before spontaneous breathing trial
Change of perfused vessel densitybaseline and 1 hourThe difference between the perfused vessel density measure by Cytocam before and after spontaneous breathing trial

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026