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The Thai Surgical Intensive Care Study (Thai-SICU Study) (THAI-SICU)

R

Royal College of Anesthesiologists of Thailand

Status

Completed

Conditions

Sequelae of External Causes of Morbidity and Mortality
Adverse Reaction to Drug
Critical Illness
Complications of Surgical and Medical Care: General Terms

Study type

Observational

Funder types

Other

Identifiers

NCT01354197
40-53-11

Details and patient eligibility

About

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.

Full 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

Enrollment

4,652 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All SICU admission patients

Exclusion criteria

  • Age < 18 years

Trial design

4,652 participants in 1 patient group

All ICU admission patients
Description:
All ICU admission to surgical intensive care unit at cohort time

Trial contacts and locations

9

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Data sourced from clinicaltrials.gov

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