- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04850248
Scoring Model for Predicting Outcome in Patients With Cardiogenic Shock
April 18, 2021 updated by: National Taiwan University Hospital
Scoring Model for Predicting Outcome in Patients With Cardiogenic Shock: From Emergency Room to Intensive Care Unit
This study aims to develop a predictive model for the outcomes of patients with cardiogenic shock
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
This retrospective observational study will enroll patients with cardiogenic shock admitted to the cardiac care unit.
Patient characteristics, clinical events during hospitalization, and laboratory examination findings will be collected and analyzed to determine factors associated with mortality.
A nomogram will be developed accordingly and will undergo both internal and external validation.
Study Type
Observational
Enrollment (Anticipated)
999
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Min-Shan Tsai, MD, PhD
- Phone Number: 65632 02-23123456
- Email: mshanmshan@gmail.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
This study will enroll patients with who arrived at the emergency department with cardiogenic shock and subsequently admitted to the cardiac care unit.
Description
Inclusion Criteria:
- Patients with cardiogenic shock
- Admitted to the cardiac care unit (CCU)
Exclusion Criteria:
- Non-cardiogenic shock in origin
- Post open heart surgery
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Mortality
Time Frame: through study completion, an average of 1 year
|
In-hospital mortality
|
through study completion, an average of 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
July 1, 2021
Primary Completion (Anticipated)
June 1, 2022
Study Completion (Anticipated)
June 1, 2022
Study Registration Dates
First Submitted
April 14, 2021
First Submitted That Met QC Criteria
April 18, 2021
First Posted (Actual)
April 20, 2021
Study Record Updates
Last Update Posted (Actual)
April 20, 2021
Last Update Submitted That Met QC Criteria
April 18, 2021
Last Verified
April 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202103043RIND
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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