- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02864459
The Role of Muscular Ultrasound in Predicting Weaning Success
August 18, 2021 updated by: Jinwoo Lee, Seoul National University Hospital
When attempting to wean a patient from the ventilator, even if he/she passes the spontaneous breathing test, 10-20% of the time extubation failure occurs and the patient is reintubated.
When the patient is reintubated the mortality rate increases and the length of intensive care unit stay is also increased.
It is vital to intensively assess the patient before extubation and correctly predict extubation success.
Muscular ultrasound may be helpful in these situations.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
114
Phase
- Not Applicable
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
-
-
-
Seoul, Korea, Republic of
- Seoul National University
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Adult patients undergoing weaning from mechanical ventilation
- Patients who have been mechanically ventilated for more than 72 hrs
Exclusion Criteria:
- Pregnant patients
- Patients with previous neuromuscular diseases
- Difficulties in muscular ultrasound (Dressing, operation, etc)
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
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Muscular ultrasound
|
Muscular ultrasound is done before extubation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Extubation success (no need for reintubation)
Time Frame: 48 hours after extubation
|
48 hours after extubation
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Weaning success (no need for applying the ventilator again)
Time Frame: 2 hours after spontaneous breathing trial
|
2 hours after spontaneous breathing trial
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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
August 1, 2016
Primary Completion (Anticipated)
December 1, 2022
Study Completion (Anticipated)
December 1, 2022
Study Registration Dates
First Submitted
August 7, 2016
First Submitted That Met QC Criteria
August 10, 2016
First Posted (Estimate)
August 12, 2016
Study Record Updates
Last Update Posted (Actual)
August 24, 2021
Last Update Submitted That Met QC Criteria
August 18, 2021
Last Verified
August 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 690 (National Heart, Lung, and Blood Institute)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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