- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07210866
- Original Trial
An Artificial Intelligence Model for Intensive Care Length of Stay, Neurological Outcome and Costs Estimation After Cardiopulmonary Resuscitation: a Cohort Study.
September 30, 2025 updated by: Nıgar Kangarlı, Bezmialem Vakif University
AN ARTIFICIAL INTELLIGENCE MODEL FOR INTENSIVE CARE LENGTH OF STAY, NEUROLOGICAL OUTCOME AND COSTS ESTIMATION AFTER CARDIOPULMONARY RESUSCITATION: A COHORT STUDY
The study aims to overview patients registered to Bezmialem Vakıf University Hospital Intensive Care Unit after successive cardiac arrest resuscitation from October 2010 to September 2025.
The goal is to determine length of stay in reanimation, neurological clinical outcome and costs of these patients at discharge from the department.
All these data is intended to be evaluated by artificial intelligence to evaluate a predictive model.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
5000
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
Patients above 18 years after successful cardiopulmonary resuscitation with ROSC registered at Bezmialem Vakıf University Hospital Intensive care unit from October 2010 to September 2025 will be included in the resesarch.
Description
Inclusion Criteria:
- age>18 years
- successive cardiopulmonary resuscitation
- at least 1 hour long admission to ICU after Return Of Spontaneous Circulation (ROSC)
Exclusion Criteria:
- age < 18 years
- >80% missing data in patient records
- patients with no ROSC
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Age >18 years patients after successful cardiopulmonary resuscitation observed in reanimation
|
Data from patients after successive rescucitaion will be evaluated by machine learning programs.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Machine Learning Python programme
Time Frame: 3 months
|
The created database will be analyzed using a machine learning artificial intelligence algorithm with the Python programming language.
After processing missing and incomplete data by artificial intelligence, the database will be divided into two parts: model training and model validation.
Meaningful data will be selected through model training, and a prediction model will be built based on these data.
To increase the interpretability of the prediction model and help users understand how and why certain predictions are made, the SHapley Additive exPlanations (SHAP) algorithm will be used.
In machine learning, the SHAP technique is used to interpret the decision-making processes of complex machine learning models.
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Estimated)
October 1, 2025
Primary Completion (Estimated)
December 1, 2025
Study Completion (Estimated)
December 1, 2025
Study Registration Dates
First Submitted
September 30, 2025
First Submitted That Met QC Criteria
September 30, 2025
First Posted (Estimated)
October 7, 2025
Study Record Updates
Last Update Posted (Estimated)
October 7, 2025
Last Update Submitted That Met QC Criteria
September 30, 2025
Last Verified
September 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Nkangarli002
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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