Development and Validation of an Interpretable Machine Learning Model for Predicting Venous Thromboembolism(VTE)in Intensive Care Unit (ICU) Patients

May 18, 2026 updated by: Weiwei Wu, Beijing Tsinghua Chang Gung Hospital
Venous thromboembolism remains a leading cause of preventable mortality in intensive care unit (ICU) patients. Existing risk-stratification tools were developed in general medical populations and lack ICU-specific predictors. This study was to develop and validate an interpretable machine learning (ML) model to predict VTE in ICU patients.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

12061

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Beijing Municipality
      • Beijing, Beijing Municipality, China, 102218
        • Beijing Tsinghua Changgung Hospital

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

Non-Probability Sample

Study Population

Patients admitted to ICU were included in the study cohort from January 2022 to October 2025. Inclusion criteria were: (1) age ≥18 years; (2) ICU length of stay ≥48 hours; (3) only the first ICU admission per patient was retained. Exclusion criteria were: (1) VTE diagnosed prior to ICU admission; (2) VTE diagnosed within 24 hours of ICU admission; (3) >20% missing values in key variables. The final cohort comprised 12,061 patients, of whom 587 (4.9%) developed VTE during ICU hospitalization.

Description

Inclusion Criteria:

  • age ≥18 years;
  • ICU length of stay ≥48 hour
  • the first ICU admission

Exclusion Criteria:

  • VTE diagnosed prior to ICU admission
  • VTE diagnosed within 24 hours of ICU admission
  • >20% missing values in key variables

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
Time Frame
validate an interpretable machine learning (ML) model to predict VTE in ICU patients
Time Frame: the first day after the patients leaf ICU
the first day after the patients leaf ICU

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 (Actual)

January 1, 2022

Primary Completion (Actual)

December 31, 2025

Study Completion (Actual)

December 31, 2025

Study Registration Dates

First Submitted

May 12, 2026

First Submitted That Met QC Criteria

May 18, 2026

First Posted (Actual)

May 19, 2026

Study Record Updates

Last Update Posted (Actual)

May 19, 2026

Last Update Submitted That Met QC Criteria

May 18, 2026

Last Verified

January 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 19242-2-01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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