- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07380607
Double Triggering Asynchrony in Mechanically Ventilated Patients.
April 10, 2026 updated by: Mansoura University
Sensitivity of Diaphragmatic Ultrasonography in Detecting Double Triggering Asynchrony in Mechanically Ventilated ICU Patients.
This observational study examined double triggering asynchrony in28ICU patients on mechanical ventilation.
Researchers collected data on patient characteristics, health conditions, and outcomes to understand how this problem affects critically ill patients.
Findings may help improve ventilator care in intensive care units.
Study Overview
Status
Completed
Study Type
Observational
Enrollment (Actual)
28
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
-
-
Dakahlia Governorate
-
Al Mansurah, Dakahlia Governorate, Egypt, 35516
- Specialised Medical Hospital - ICU
-
-
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
Adult patients (>18 years) admitted to medical/surgical ICU at Specialized Medical Hospital, Mansoura University, receiving invasive mechanical ventilation with documented double triggering asynchrony on ventilator waveform analysis.
Description
Inclusion Criteria:
- Adult ICU patients aged ≥18 years receiving invasive mechanical ventilation
- Documented double triggering asynchrony on ventilator waveform analysis.
Exclusion Criteria:
- Patients with contraindications to diaphragmatic ultrasound, including thoracic or abdominal surgery.
- Patients with known diseases affecting diaphragmatic function, such as Duchenne muscular dystrophy (DMD) or myasthenia gravis (MG).
- Patients with advanced chronic liver disease (Child-Pugh class C)
- Patients with chronic increased intra-abdominal pressure.
- Patients with moderate to massive pleural effusion.
- Patient or legal guardian refusal to participate in the study.
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 |
|---|
|
Double Triggering Cohort
28mechanically ventilated ICU patients identified with double triggering asynchrony
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sensitivity of diaphragmatic ultrasound for detection of double triggering asynchrony
Time Frame: During ICU admission, at the time of double triggering detection by ventilator graph interpretation
|
Proportion of double triggering asynchrony events correctly identified by diaphragmatic ultrasound compared with ventilator waveform analysis as the reference standard
|
During ICU admission, at the time of double triggering detection by ventilator graph interpretation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
November 5, 2024
Primary Completion (Actual)
October 20, 2025
Study Completion (Actual)
November 2, 2025
Study Registration Dates
First Submitted
January 17, 2026
First Submitted That Met QC Criteria
January 24, 2026
First Posted (Actual)
February 2, 2026
Study Record Updates
Last Update Posted (Actual)
April 15, 2026
Last Update Submitted That Met QC Criteria
April 10, 2026
Last Verified
December 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- MD.24.03.838.R1
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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