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Clinical Trials/TCTR20210607003
TCTR20210607003
Not yet recruiting
Phase 1

Effects of Nasal Continuous Positive Airway Pressure Compared with High Flow Nasal Cannula on The Coordination Between Swallowing and Breathing in Post-extubation Patients, a Randomized Crossover Study

Ratchadapisek Research Funds, Faculty of Medicine, Chulalongkorn University0 sites26 target enrollmentJune 7, 2021
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ConditionsSwallowing- breathing coordination in postextubation patients using nasal continuous positive airway pressure and high flow nasal cannulanasal continuous positive airway pressurehigh flow nasal cannulaswallowing and breathing coordinationpostextubation patients

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Swallowing- breathing coordination in postextubation patients using nasal continuous positive airway pressure and high flow nasal cannula
Sponsor
Ratchadapisek Research Funds, Faculty of Medicine, Chulalongkorn University
Enrollment
26
Status
Not yet recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 7, 2021
End Date
June 30, 2022
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Ratchadapisek Research Funds, Faculty of Medicine, Chulalongkorn University

Eligibility Criteria

Inclusion Criteria

  • •1\. intubated for more than 48 hours and extubated within 48 hours
  • •2\. able to maintain adequate oxygen saturation by using low flow oxygen cannula 1\-5 LPM
  • •3\. have stable vital signs
  • •4\. pass the modified swallowing test with the score of more than 3 points

Exclusion Criteria

  • •1\. not cooperative
  • •2\. have contraindication for enteral feeding
  • •3\. cerebrovascular disease, neuromuscular disease or muscle weakness
  • •4\. head and neck cancer
  • •5\. structural abnormalities of oral cavity or pharynx
  • •6\. history of surgery within oral cavity or pharyngeal area
  • •7\. delirium
  • •8\. previous diagnosis of dysphagia
  • •9\. skin lesions which interfered with EMG monitoring
  • •10\. have automated implantable cardioverter\-defibrillator or permanent pacemaker

Outcomes

Primary Outcomes

Not specified

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