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Epidemiology of Sepsis in Turkish ICUs.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03249246
Recruitment Status : Completed
First Posted : August 15, 2017
Last Update Posted : August 15, 2017
Sponsor:
Collaborator:
Turkish Society of Intensive Care, Sepsis Study Group
Information provided by (Responsible Party):
Nur Baykara, Turkish Intensive Care Society

Brief Summary:
The prevalence and mortality of sepsis in Turkey is not know at large. Turkish Society of Intensive Care Medicine, Sepsis Study Group conducted a multi-centre,point prevalence survey to determine the prevalence, causative micro-organisms and outcome of sepsis in Turkish ICUs.

Condition or disease Intervention/treatment
Sepsis Septic Shock Severe Sepsis Other: No intervention

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Study Type : Observational
Actual Enrollment : 1499 participants
Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Epidemiology of Sepsis in Turkish ICUs :a National Point Prevalence Multi-centre Study.
Actual Study Start Date : January 27, 2016
Actual Primary Completion Date : January 28, 2016
Actual Study Completion Date : February 27, 2016

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Sepsis

Group/Cohort Intervention/treatment
Infection only
The patients have only infection
Other: No intervention
Infection + SIRS
Patients have infection plus systemic inflammatory response syndrome (SIRS)
Other: No intervention
Severe sepsis
Septic patients with newly developed organ dysfunctions
Other: No intervention
Septic shock
Sepsis plus sepsis related hypotension
Other: No intervention



Primary Outcome Measures :
  1. Prevalence of sepsis [ Time Frame: Up to 12 weeks. ]
    The prevalence of sepsis,Severe sepsis and septic shock on study day


Secondary Outcome Measures :
  1. Mortality rate of sepsis [ Time Frame: Mortality at 30 days ]
    Mortality rate of septic shock



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
All patients (>18 yr)present on the participating ICU or admitted to participating ICUs on study day
Criteria

Inclusion Criteria:All patients present on or admitted to participating ICU on study day.

Exclusion Criteria:

  • Age<18 years
  • Patients who underwent cardiovascular surgery.
Publications of Results:
Other Publications:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Nur Baykara, Prof.Dr.Nur Baykara, Turkish Intensive Care Society
ClinicalTrials.gov Identifier: NCT03249246    
Other Study ID Numbers: TurkishICS
First Posted: August 15, 2017    Key Record Dates
Last Update Posted: August 15, 2017
Last Verified: August 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Nur Baykara, Turkish Intensive Care Society:
Sepsis
ICU
Point prevalence
Additional relevant MeSH terms:
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Sepsis
Toxemia
Infection
Systemic Inflammatory Response Syndrome
Inflammation
Pathologic Processes