Comparison of the Decannulation Protocol With Suctioning and Capping in Severe Acquired Brain Injury Patients
NCT ID: NCT04835272
Last Updated: 2021-10-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
104 participants
INTERVENTIONAL
2021-11-01
2023-10-30
Brief Summary
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1. an assessment of readiness for decannulation that was based on suctioning frequency
2. an assessment that was based on tracheostomy capping
Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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control group
In the control group, the decision to decannulate was based on a 48-hour capping trial.
No interventions assigned to this group
intervention group
In the intervention group, the decision to decannulate was based on suctioning frequency.
the Decannulation Protocol With Suctioning
In the intervention group, the decision to decannulate was based on suctioning frequency. Patients underwent decannulation when they had had no more than two aspirations every 8 hours during during a 24-hour period. Patients in this group did not undergo capping trials.
Interventions
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the Decannulation Protocol With Suctioning
In the intervention group, the decision to decannulate was based on suctioning frequency. Patients underwent decannulation when they had had no more than two aspirations every 8 hours during during a 24-hour period. Patients in this group did not undergo capping trials.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Age≥18 years old
* GCS≥8
* Clinical stability( defined as the absence of fever, sepsis, or active infection and hemodynamic stability)
* Without massive pooling or silent aspiration of saliva, more than one efficient swallow per minute, adequate cough reflex were tested by gently touching the aryepiglottic region with the tip of the endoscope.
* Passing a tracheostomy-tube de-cuff test(de-cuff the tube for 3 days without pulmonary complications.
* Without significant airway stenosis.
Exclusion Criteria
* Medical history of severe respiratory system or heart disease
* Neuromuscular disease other than ICU-acquired weakness, or tracheostomy for airway control
* Don't get informed consent from patient or guardian
18 Years
ALL
No
Sponsors
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Fu Xing Hospital, Capital Medical University
OTHER
Responsible Party
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Song Lu
Attending doctor
Principal Investigators
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Yong Wang
Role: STUDY_CHAIR
Rehabilitation medicine center, Fuxing hospital, capital medical university
Locations
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Fuxing hospital, capital medical university
Beijing, , China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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songlu20210320
Identifier Type: -
Identifier Source: org_study_id