NCT06751693

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
25,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Dec 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 10, 2024

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

December 11, 2024

Completed
13 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 24, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 24, 2024

Completed
6 days until next milestone

First Posted

Study publicly available on registry

December 30, 2024

Completed
Last Updated

December 30, 2024

Status Verified

December 1, 2024

Enrollment Period

14 days

First QC Date

December 11, 2024

Last Update Submit

December 26, 2024

Conditions

Keywords

Deep Learning

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

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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)

Location

MeSH Terms

Conditions

Acute Lung Injury

Condition Hierarchy (Ancestors)

Lung InjuryLung DiseasesRespiratory Tract Diseases

Study Officials

  • Zafer Cukurova, M.D

    Bakırkoy Dr. Sadi Konuk Training and Research Hospital

    STUDY CHAIR

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

Locations