Evaluation of Effectiveness of Blue Code Team After In-hospital Cardiopulmonary Arrest (Codeblue)
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| ClinicalTrials.gov Identifier: NCT03378518 |
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Recruitment Status :
Completed
First Posted : December 20, 2017
Last Update Posted : December 21, 2017
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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 2016-2017.
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 2016-2017.
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.
| Condition or disease |
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| In-hospital Cardiac Arrest |
This study aimed to retrospectively examine patients evaluated by the Code Blue team on a Code Blue call in our hospital between 20016 and 2017.
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 2016-2017.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.
| Study Type : | Observational |
| Actual Enrollment : | 264 participants |
| Observational Model: | Other |
| Time Perspective: | Retrospective |
| Official Title: | Evaluation of Effectiveness of Blue Code Team After In-hospital Cardiopulmonary Arrest |
| Actual Study Start Date : | January 1, 2016 |
| Actual Primary Completion Date : | December 31, 2016 |
| Actual Study Completion Date : | July 1, 2017 |
- Blue code notification form [ Time Frame: 12 month ]Survival rate of patients intervened by blue code team after in-hospital cardiac arrest
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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: | Non-Probability Sample |
Inclusion criteria:
-Patients intervened by code blue team
Exclusion criteria:
- Cardiac arrest in the anesthesiology and reanimation intensive care unit
- Cardiac arrest in the newborn intensive care unit
- Out-of-hospital cardiac arrest
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): NCT03378518
| Turkey | |
| Adnan Menderes University Training and Research Hospital | |
| Aydın, Turkey, 09100 | |
| Principal Investigator: | sinan yılmaz | Aydin Adnan Menderes University |
| Responsible Party: | SİNAN YILMAZ, Assistant Professor, Aydin Adnan Menderes University |
| ClinicalTrials.gov Identifier: | NCT03378518 |
| Other Study ID Numbers: |
Codeblue |
| First Posted: | December 20, 2017 Key Record Dates |
| Last Update Posted: | December 21, 2017 |
| Last Verified: | November 2017 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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In-hospital Cardiac Arrest, mortality |
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Heart Arrest Heart Diseases Cardiovascular Diseases |

