NCT05026437

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
204

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2019

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 2, 2019

Completed
21 days until next milestone

First Submitted

Initial submission to the registry

January 23, 2019

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 10, 2019

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

April 10, 2019

Completed
2.4 years until next milestone

First Posted

Study publicly available on registry

August 30, 2021

Completed
Last Updated

August 30, 2021

Status Verified

August 1, 2021

Enrollment Period

2 months

First QC Date

January 23, 2019

Last Update Submit

August 23, 2021

Conditions

Keywords

cardiac surgery score, mortality, ICU

Outcome Measures

Primary Outcomes (2)

  • Mortality at 7 days

    Mortality in the first 7 days after surgery

    7 days

  • Mortality at 30 days

    Mortality in the first 30 days after surgery

    30 days

Secondary Outcomes (2)

  • Length of stay in the cardiac intensive care unit

    Up to 3 months (Through study completion)

  • Length of the stay in the hospital

    Up to 3 months (Through study completion)

Interventions

Cardiac surgery score and APACHE II will calculated on the first postoperative day.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Study population includes all adult patients who undergoing coronary artery bypass grafting during the study period.

You may qualify if:

  • Undergoing coronary artery bypass grafting
  • Over 18 years of age
  • Staying at least 24 hours in the cardiac intensive care unit

You may not qualify if:

  • Emergency surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital in Turkey

Istanbul, Turkey (Türkiye)

Location

Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital

Istanbul, Turkey (Türkiye)

Location

Study Officials

  • Nihan YAPICI

    Dr. Siyami Ersek Thoracic and Cardiovascular Surgery TRH

    STUDY DIRECTOR
  • Sümeyye UĞUR

    Haydarpaşa Numune Training and Research Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Target Duration
1 Month
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
drsumeyyeugur@gmail.com

Study Record Dates

First Submitted

January 23, 2019

First Posted

August 30, 2021

Study Start

January 2, 2019

Primary Completion

March 10, 2019

Study Completion

April 10, 2019

Last Updated

August 30, 2021

Record last verified: 2021-08

Locations