Development of a Scoring and Prediction Model for Weaning Success in ARDS Patients Using Ventilation Parameters Combined with Artificial Intelligence and Deep Learning Techniques
1 other identifier
observational
25,000
1 country
1
Brief Summary
This study aims to develop an AI-supported scoring model to optimize the weaning processes of ARDS patients from mechanical ventilation. Retrospective analysis will be conducted on the data of 25,000 patients, focusing on ventilator parameters and hemodynamic variables. The model will be designed to contribute to clinical decision support systems.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 10, 2024
CompletedFirst Submitted
Initial submission to the registry
December 11, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 24, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 24, 2024
CompletedFirst Posted
Study publicly available on registry
December 30, 2024
CompletedDecember 30, 2024
December 1, 2024
14 days
December 11, 2024
December 26, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Successful Weaning
The primary outcome of this study will be the successful weaning from mechanical ventilation.
48 hours
Secondary Outcomes (1)
Mechanical Ventilatory Parameters
48 hours
Study Arms (2)
Weaned
Those successfully weaned from mechanical ventilation
Non-weaned
Those who not weaned from mechanical ventilation
Eligibility Criteria
Intubated patients which diagnosed with ARDS and followed up in the ICU for more than 48 hours.
You may qualify if:
- ARDS diagnosis
- Aged 18 years and older
- Intubated and followed by Mechanical ventilation
- Admission on Intensive care unit
- Complete data on clinical support and desicion system
You may not qualify if:
- Missing data
- Under 18 years of age
- Followed by non-ARDS conditions
- Terminal status
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bakirkoy Dr Sadi Konuk Research and Training Hospital
Istanbul, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Zafer Cukurova, M.D
Bakırkoy Dr. Sadi Konuk Training and Research Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 11, 2024
First Posted
December 30, 2024
Study Start
December 10, 2024
Primary Completion
December 24, 2024
Study Completion
December 24, 2024
Last Updated
December 30, 2024
Record last verified: 2024-12
Data Sharing
- IPD Sharing
- Will not share