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Clinical Trials/NCT06000995
NCT06000995
Completed
Not Applicable

Determination of Fiberoptic Bronchoscopy Sedation Protocols; Survey Study on Sedation Attitudes and Behaviors of Chest Diseases Specialists in Turkey

Samsun University1 site in 1 country97 target enrollmentMay 16, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fiberoptic Bronchoscopy
Sponsor
Samsun University
Enrollment
97
Locations
1
Primary Endpoint
FOB related survey questions
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Fiberoptic bronchoscopy (FOB), which is difficult to tolerate while awake, is recommended to be performed by the patient under sedation. The aim of this study is to determine the attitudes and behaviors of chest diseases specialists who do FOB in Turkey about sedation with a 30-question online questionnaire.

Detailed Description

Fiberoptic bronchoscopy is the imaging of the tracheobronchial tree for diagnosis and treatment in lung diseases. The operation performed through the airway is difficult for the patient to tolerate. Therefore, it is recommended to perform the procedure under sedation. With this survey study, it was aimed to determine the sedation protocols preferred by pulmonologists who perform active fiberoptic bronchoscopy throughout Turkey during the procedure. Thirty questions were determined for the questionnaire to be used as a data collection method by the researchers. The questions generally consist of three parts; In the first part, there are 8 questions containing the personal information of the doctors (age, gender, title, institution, etc.). In the second part, 13 questions were included in order to make a general assessment such as the sedative agents used by the doctors before and during the bronchoscopy procedure, and the satisfaction with the sedative method used. In the third part, 9 questions were given to determine the preferred follow-up methods during the procedure. The questions are designed to be presented to participants over the network using google forms.

Registry
clinicaltrials.gov
Start Date
May 16, 2022
End Date
July 31, 2022
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Samsun University
Responsible Party
Principal Investigator
Principal Investigator

dilan akyurt

Principle investigator

Samsun University

Eligibility Criteria

Inclusion Criteria

  • Currently working as a pulmonologist

Exclusion Criteria

  • Not actively performing fiberoptic bronchoscopy for the past five years

Outcomes

Primary Outcomes

FOB related survey questions

Time Frame: 15 minutes

The pulmonologists' responses to 30 questionnaire questions were recorded. Thirty questions generally consisted of three parts; Part 1; personal information of doctors (age, gender, title, institution, etc.), in section 2; sedative agents used by doctors before and during bronchoscopy and satisfaction with the sedative method used, part 3; preferred follow-up methods during the procedure.

Study Sites (1)

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