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NCT05026437 Clinical Trial

CASUS vs. APACHE II in Predicting Mortality After Coronary Artery Bypass Grafting

Mortality Clinical Trial

— CASUS  

Official title:
The Value of CASUS vs. APACHE II in Predicting Mortality Among Patients Undergoing Coronary Artery Bypass Grafting

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05026437
Other study ID # SU2019
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2, 2019
Est. completion date April 10, 2019

Study information
Verified date August 2021
Source Antalya Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The study seeks to determine the value of CASUS in predicting mortality as compared with APACHE II scoring system among patients undergoing coronary artery bypass grafting.

Description:

Patients undergoing coronary artery bypass grafting will prospectively studied after the admission to the cardiac intensive care unit. Data on the preoperative condition, intraoperative parameters, and postoperative course will collected. CASUS and APACHE II scores will calculated on the first postoperative day. Clinical outcomes are defined as 7-day mortality, 30-day mortality and morbidity. Morbidity includes variables such as length of stay in the cardiac surgical intensive care unit and in the hospital.

Recruitment information / eligibility
Status Completed
Enrollment 204
Est. completion date April 10, 2019
Est. primary completion date March 10, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Undergoing coronary artery bypass grafting - Over 18 years of age - Staying at least 24 hours in the cardiac intensive care unit Exclusion Criteria: - Emergency surgery

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Cardiac surgery score and APACHE II scoring
Cardiac surgery score and APACHE II will calculated on the first postoperative day.

Locations
Country Name City State
Turkey Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital Istanbul
Turkey Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital in Turkey Istanbul

Sponsors (3)
Lead Sponsor Collaborator
Antalya Training and Research Hospital Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital, Haydarpasa Numune Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Mortality at 7 days Mortality in the first 7 days after surgery 7 days
Primary Mortality at 30 days Mortality in the first 30 days after surgery 30 days
Secondary Length of stay in the cardiac intensive care unit Only the length of the initial stay in the cardiac intensive care unit up to 3 months Up to 3 months (Through study completion)
Secondary Length of the stay in the hospital It includes the period from surgery to discharge Up to 3 months (Through study completion)
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