- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06582407
Machine Learning Models for Predicting Unforeseen Hospital Admissions or Discharges After Anesthesia
October 16, 2024 updated by: Rémi Florquin, HUmani
Unexpected hospital admissions after ambulatory surgery not only bring discomfort to patients but also causes a decrease in the efficiency of the healthcare system.
In addition, unanticipated patient's orientation carry the risk of unsuitable post operative orders.
The hypothesis of this project is that artificial intelligence models will outperform traditional models in predicting which patients will require hospital admission after ambulatory surgery or unforeseen hospital discharge after surgery.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
68683
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
-
-
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Mons, Belgium, 7000
- Université de Mons
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
All hospitalized or outpatient patients who have undergone anesthesia for a diagnostic or therapeutic procedure, in a scheduled or emergency condition, in the institution's hospitals.
Description
Inclusion Criteria:
- Patient undergoing anesthesia for a therapeutic or diagnostic procedure
Exclusion Criteria:
- Incomplete informatic data
- Error in the encoding system
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 |
|---|---|
|
Ambulatory Patients
Patient undergoing anesthesia in an ambulatory setting.
|
The goal of this project is to develop models to predict in the preoperative period which patients will require hospital admission after ambulatory surgery or unforeseen hospital discharge after surgery
|
|
Hospitalised Patients
Patient undergoing anesthesia in a hospitalisation setting.
|
The goal of this project is to develop models to predict in the preoperative period which patients will require hospital admission after ambulatory surgery or unforeseen hospital discharge after surgery
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Rate of patient reorientation
Time Frame: On the day of the operation
|
Rate of unforeseen hospital admission after an ambulatory surgery and rate of discharge after an hospitalised surgery
|
On the day of the operation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Rémi Florquin, MD, Université de Mons, Belgium
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, 2020
Primary Completion (Actual)
June 30, 2024
Study Completion (Actual)
July 30, 2024
Study Registration Dates
First Submitted
August 30, 2024
First Submitted That Met QC Criteria
August 30, 2024
First Posted (Actual)
September 3, 2024
Study Record Updates
Last Update Posted (Actual)
October 18, 2024
Last Update Submitted That Met QC Criteria
October 16, 2024
Last Verified
October 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HUmani_ODanesth
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
The investigators are not authorized to publish sensitive data by decision of the ethics committee
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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