Can Total Mechanical Power Be a Determinant of Weaning Failure in Chronic Obstructive Pulmonary Disease (COPD)?
1 other identifier
observational
1,000
1 country
1
Brief Summary
A Comparison of Ventilator Parameters (TV, DP, Total Mechanical Power, etc.) Between Successfully and unsuccessfully Weaned Patients with COPD Undergoing Mechanical Ventilation Due to Respiratory Failure, and Diagnosed with Pneumonia or ARDS in the Intensive Care Unit."
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
Shorter than P25 for all trials
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 6, 2024
CompletedFirst Submitted
Initial submission to the registry
December 11, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 23, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 23, 2024
CompletedFirst Posted
Study publicly available on registry
December 30, 2024
CompletedDecember 30, 2024
December 1, 2024
17 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. This will be defined as the patient being successfully extubated and maintaining adequate oxygenation for more than 48 hours without requiring reintubation or mechanical ventilation support.
48 hours
Secondary Outcomes (1)
Mechanical Ventilator Parameters
48 hours
Study Arms (2)
Weaned
patients with successful weaning from mechanic ventilator
Non-weaned
patients who have failed to wean from ventilator
Eligibility Criteria
Intubated patients with COPD which has been diagnosed Pneumonia or ARDS and have admission to icu and stayed for more than 5 years.
You may qualify if:
- Patients aged 18 years and older
- COPD-diagnosed patients who have been intubated and stayed in the ICU for more than 5 days
You may not qualify if:
- Patients without electronic medical records
- Patients under 18 years of age
- Patients diagnosed with pulmonary malignancy
- Patients who stayed in the ICU for less than 5 days
- Patients monitored in the ICU without intubation
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 DIRECTOR
Seyed Mohammadreza Hashemian, M.D
Masih Daneshvari 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 6, 2024
Primary Completion
December 23, 2024
Study Completion
December 23, 2024
Last Updated
December 30, 2024
Record last verified: 2024-12
Data Sharing
- IPD Sharing
- Will not share