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Data Registry of Intensive Care Unit (ICU) Siamitra and Intensive Care Unit (ICU) Salad-Samung

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified May 2011 by Mahidol University.
Recruitment status was:  Recruiting
Information provided by:
Mahidol University Identifier:
First received: May 25, 2011
Last updated: NA
Last verified: May 2011
History: No changes posted
As 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 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 for 1 years to explore the adequacy of these ICUs services, resource utilization (ICU length of stay and ventilator day), ICU complications and adverse outcome /ICU readmission within 72 hours after discharging from ICU.


Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Data Registry of ICU Siamitra and ICU Salad-Samung

Further study details as provided by Mahidol University:

Primary Outcome Measures:
  • Incidence of ICU refusal [ Time Frame: 1 years ]
    The primary outcome measure of this study is the incidence of ICU refusal

Secondary Outcome Measures:
  • ICU complication, resource utilization and adverse events/ICU readmission within 72 hours after discharging from ICU [ Time Frame: 1 years ]
    The secondary outcomes of this study are to study ICU complication, resource utilization and adverse events/ICU admission within 72 hours after discharging from ICU

Estimated Enrollment: 1000
Study Start Date: May 2011
Estimated Study Completion Date: May 2012
Estimated Primary Completion Date: April 2012 (Final data collection date for primary outcome measure)
complication, refusal ICU admission, adverse event


Ages Eligible for Study:   19 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Adult (> 18 years), admitting to ICU Siamitra and ICU Salad-Samung

Inclusion Criteria:

  • Age > 18 years
  • Surgical patients
  • Written informed consent to this study

Exclusion Criteria:

  • Patient undergoing cardiothoracic surgery, traumatic surgery, neurosurgery
  • Not consent to this study
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01361477

ICU Siamitra and ICU Salad-Samung, Siriraj Hospital, Mahidol University
Bangkoknoi, Bangkok, Thailand, 10700
ICU Siamitra and ICU Salad-Samung, Siriraj Hospital
Bangkoknoi, Bangkok, Thailand, 10700
Sponsors and Collaborators
Mahidol University
Principal Investigator: Suneerat Kongsereepong, MD Mahidol University
  More Information

Responsible Party: Prof. Suneerat Kongsereepong, MD, Siriraj Hospital, Mahidol University, Bangkok, Thailnad Identifier: NCT01361477     History of Changes
Other Study ID Numbers: Si227/2011 
Study First Received: May 25, 2011
Last Updated: May 25, 2011

Keywords provided by Mahidol University:
General surgical ICU
ICU Siamitra
ICU Salad-Samung
Data registry
ICU refusal
ICU complications
ICU resource utilization
Adverse events
ICU readmission processed this record on February 20, 2017