Perfusion IndexWeaning of Mechanical VentilationICU
Investigational drug(s) / intervention(s)
patients were monitored for reentubation for 48 hours.weaning group
patients were monitored for reentubation for 48 hours.: patients were monitored for reentubation for 48 hours.
weaning group: patients were monitored for reentubation for 48 hours.
Study summary
The aim of this study is to evaluate the predictive role of the Peripheral Perfusion Index (PPI) in forecasting extubation success during the weaning process in intensive care unit (ICU) patients. The study will investigate the ability of PPI to predict extubation failure by comparing it with traditional weaning criteria, including the Rapid Shallow Breathing Index (RSBI), PaO₂/FiO₂ ratio, and respiratory rate.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Patients who have been on mechanical ventilation for at least 48 hours
* Patients over 18 years of age who are planned to undergo extubation following a spontaneous breathing trial (SBT)
* Patients or their legal representatives who provide informed consent to participate in the study
Exclusion Criteria:
* Patients for whom extubation is not planned due to hemodynamic instability
* Patients with peripheral vascular disease or a history of hand surgery
* Patients who die or cannot be followed up during the study period
Primary outcome measure(s)
• The ability of Peripheric Perfusion Index(PPI) measured 1 hour after extubation to predict extubation failure within 48 hours following extubation. — 48 hours
Trial sites (1)
Facility
City
Region
Status
Gaziosmanpaşa Training and Research Hospital
Istanbul
Turkey (Türkiye)
Recruiting
More Gaziosmanpasa Research and Education Hospital trials in Turkey
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.
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