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Clinical Trials/NCT01354197
NCT01354197
Completed
N/A

Multicenter Study of Outcome and Adverse Events in Surgical Intensive Care Unit of Thai University Hospital

Royal College of Anesthesiologists of Thailand9 sites in 1 country4,652 target enrollmentApril 2011

Overview

Phase
N/A
Intervention
Not specified
Conditions
Complications of Surgical and Medical Care: General Terms
Sponsor
Royal College of Anesthesiologists of Thailand
Enrollment
4652
Locations
9
Primary Endpoint
Overall Mortality
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The study observed the 28 days mortality of 9 participated University base surgical intensive care unit (SICU) as well as the occurrence of adverse events in SICU.

Detailed Description

The adverse events included pulmonary aspiration, pulmonary emboli, drug error, new stroke, symptomatic deep vein thrombosis, pneumothorax, unplanned extubation, upper GI hemorrhage, myocardial infarction, abdominal hypertension, acute lung injury(ALI)/acute respiratory distress syndrome (ARDS), re-intubation within 72 hours, delirium, cardiac arrest, new arrhythmia, acute kidney injury, sepsis

Registry
clinicaltrials.gov
Start Date
April 2011
End Date
January 2013
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Royal College of Anesthesiologists of Thailand
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All SICU admission patients

Exclusion Criteria

  • Age \< 18 years

Outcomes

Primary Outcomes

Overall Mortality

Time Frame: 28 days

Number of Participants who Did Not Survive up to 28 days after surgical ICU admission

Secondary Outcomes

  • Readmission to ICU(3 days)

Study Sites (9)

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