Status:
COMPLETED
This Study Will Evaluate the Effectiveness of a Simple Intervention Through a Classical Yankauer Oral Suction Tube, in Decreasing the Sedative Medication Doses Needed to Provide Effective Patient Sedation During Bronchoscopy, Along With Its Effect on Both Patient's and Bronchoscopist Satisfaction
Lead Sponsor:
American University of Beirut Medical Center
Conditions:
Bronchoscopy
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The aim of this study is to evaluate the effectiveness of a simple intervention through a classical Yankauer oral suction tube, a device known to have a proven safety profile in multiple healthcare se...
Eligibility Criteria
Inclusion
- 18 years or above
- inpatients or outpatients
- scheduled to have a flexible bronchoscopy for one of multiple indications based on their physician's assessment, including the presence of a lung mass or collapse, persistent pulmonary infiltrates, pulmonary infection in the setting of immunosuppression, hemoptysis, or other rare causes like chronic cough.
- patients provided a written informed consent.
Exclusion
- patients with anatomic oro-pharyngeal abnormalities,
- critically ill patients
- uncooperative patients or inability to provide signed consent by the patient or their legal representative
- coagulopathy or bleeding diathesis
- severe obstructive airway disease
- recent myocardial infarction
- uncontrolled or poorly controlled asthma or chronic obstructive pulmonary disease (COPD)
- pregnancy.
Key Trial Info
Start Date :
March 4 2016
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 14 2022
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT06908109
Start Date
March 4 2016
End Date
October 14 2022
Last Update
April 4 2025
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