The Patient Characteristics and Mortality of Code Blue Calls
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ClinicalTrials.gov Identifier: NCT02203435 |
Recruitment Status :
Completed
First Posted : July 29, 2014
Last Update Posted : August 6, 2014
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This study aimed to retrospectively examine patients evaluated by the Code Blue team on a Code Blue call in our hospital between 2009 and 2013.
Primary outcome: an examination of the survival rates and demographic data of the patients evaluated as an emergency by a Code Blue call in the period 2009-2013.Secondary outcome: to determine the rates of false Code Blue calls, the clinics giving Code Blue calls and the relationship between the times of Code Blue calls and mortality.Inclusion criteria: patients throughout the whole hospital for whom a Code Blue form was completed and who were evaluated by the Code Blue team on a Code Blue call.
Exclusion criteria: patients who refused treatment
Condition or disease |
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Demographics of the Patients Evaluated by Code Blue Call |
Study Type : | Observational |
Actual Enrollment : | 1050 participants |
Time Perspective: | Retrospective |
Official Title: | The Characteristics of the Blue-code Calls; Five Years Survey. |
Study Start Date : | January 2014 |
Actual Primary Completion Date : | April 2014 |
Actual Study Completion Date : | April 2014 |
- mortality of blue-codes [ Time Frame: 5 years ]an examination of the survival rates and demographic data of the patients evaluated as an emergency by a Code Blue call in the period 2009-2013.
- the demographics of blue code admissions [ Time Frame: 5 years ]to determine the rates of false Code Blue calls, the clinics giving Code Blue calls and the relationship between the times of Code Blue calls and mortality.
- the rate of successful cardiopulmonary resuscitation [ Time Frame: 5 years ]the rate of CPR, the apache and saps II expanded values and indication of ICU stay will be calculated

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Ages Eligible for Study: | Child, Adult, Older Adult |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
Patients throughout the whole hospital for whom a Code Blue form was completed and who were evaluated by the Code Blue team on a Code Blue call.
Exclusion Criteria:
Patients who refused treatment
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To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02203435
Turkey | |
Istanbul Umraniye Education and Research Hospital | |
Istanbul, Turkey, 34760 |
Study Director: | Nurten Bakan, assoc prof | Istanbul Umraniye Education and Research Hospital |
Other Publications:
Responsible Party: | Gulsah Karaoren, doctor, Umraniye Education and Research Hospital |
ClinicalTrials.gov Identifier: | NCT02203435 |
Other Study ID Numbers: |
GK1 |
First Posted: | July 29, 2014 Key Record Dates |
Last Update Posted: | August 6, 2014 |
Last Verified: | August 2014 |
code blue Cardiopulmonary Resuscitation APACHE |