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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01361477
Other study ID # Si227/2011
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 2011
Est. completion date September 2024

Study information

Verified date October 2023
Source Mahidol University
Contact Suneerat Kongsayreepong, MD
Phone +661-8427419
Email suneerat.kon@mahidol.ac.th
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

As a general surgical intensive care units of the biggest tertiary referral university of Thailand with more than 1,000 admissions/year, recently, more complicated perioperative care surgical patients were accepted with high complications, morbidities, mortality and resource utilization. Good data registration was needed to provide information for quality improvement and resource allocation. This prospective observational (crosssectional) study was designed to register patient > 18 years who will be admitted to these ICUs to explore the adequacy of these ICUs services, resource utilization (ICU length of stay and ventilator day), ICU complications, adverse outcome /ICU readmission within 72 hours after discharging from ICU. In addition, severe hemodynamic, respiratory, or neurological disturbance or complication intra and early postoperative (within 7 days after operation) that lead to ICU admission eg, intraoperative hypotension, intraoperative cardiac arrest, perioperative pulmonary aspirtaion will also be studied.


Description:

This prospective obseverational study wae ans will be done in all surgical patient (age . 18 yeras) admitted to the general surgical ICU (ICU Siammitra and ICU Salad-sumang) of the Department of Anesthesiology, Siriraj Hospital, Faculty of Medicine, Mahidol UNiversity, Bangkok, Thailand. After approval by the IRB of Siriaj Hospital, all information of the patients admiited to the ICUs were carefully recorded included patient demographic data, comorbidities, type of anesthesia, type of surgery, complication associated with anesthesia and surgery, type of ICU admission and course in ICU including outcome as Iresouce utilization (cost in ICU, ventilator day, ICU and hosital length of stay. Morbidity occcuring in ICU, 28 and 90 days mortality also recorded.


Recruitment information / eligibility

Status Recruiting
Enrollment 2000
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria: - Age > 18 years - Surgical patients Exclusion Criteria: - Patient undergoing cardiothoracic surgery, traumatic surgery, neurosurgery

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Thailand ICU Siamitra and ICU Salad-Samung, Siriraj Hospital Bangkoknoi Bangkok
Thailand ICU Siamitra and ICU Salad-Samung, Siriraj Hospital, Mahidol University Bangkoknoi Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

References & Publications (1)

Capuzzo M, Moreno RP, Alvisi R. Admission and discharge of critically ill patients. Curr Opin Crit Care. 2010 Oct;16(5):499-504. doi: 10.1097/MCC.0b013e32833cb874. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Prolonged ICU stay Incidence and factors associated with prolonged ICU stay 9 years
Secondary ICU complication, resource utilization and adverse events/ICU readmission within 72 hours after discharging from ICU ICU complication, resource utilization and adverse events/ICU admission within 72 hours after discharging from ICU 9 years
Secondary Unplanned ICU admission All unplanned ICU Admission (from OR and from floor) 9 years
Secondary outcome of complications occurring intraoperative and admitting to ICU all complication including: intraoperative cardiac arrest, hypotension 9 years
Secondary sepsis and septic shock on ICU admission incidence, clinical course and outcome of surgical septic shock admitting to ICU 9 years
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