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Determination of Fiberoptic Bronchoscopy Sedation Protocols in Turkey

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ClinicalTrials.gov Identifier: NCT06000995
Recruitment Status : Completed
First Posted : August 21, 2023
Last Update Posted : August 21, 2023
Sponsor:
Information provided by (Responsible Party):
dilan akyurt, Samsun University

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.

Condition or disease Intervention/treatment
Fiberoptic Bronchoscopy Other: Survey Questions

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.

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Study Type : Observational
Actual Enrollment : 97 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Determination of Fiberoptic Bronchoscopy Sedation Protocols; Survey Study on Sedation Attitudes and Behaviors of Chest Diseases Specialists in Turkey
Actual Study Start Date : May 16, 2022
Actual Primary Completion Date : July 30, 2022
Actual Study Completion Date : July 31, 2022

Group/Cohort Intervention/treatment
Pulmonologists
pulmonologists actively performing fiberoptic bronchoscopy
Other: Survey Questions
Thirty 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.




Primary Outcome Measures :
  1. 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.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Pulmonologists who are still working in Turkey and have been actively doing FOB for the last 5 years
Criteria

Inclusion Criteria:

  • Currently working as a pulmonologist

Exclusion Criteria:

  • Not actively performing fiberoptic bronchoscopy for the past five years

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT06000995


Locations
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Turkey
Dilan Akyurt
Samsun, Turkey, 55270
Sponsors and Collaborators
Samsun University
Publications:
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Responsible Party: dilan akyurt, Principle investigator, Samsun University
ClinicalTrials.gov Identifier: NCT06000995    
Other Study ID Numbers: B.30.2.ODM.0.20.08/340
First Posted: August 21, 2023    Key Record Dates
Last Update Posted: August 21, 2023
Last Verified: August 2023
Keywords provided by dilan akyurt, Samsun University:
sedation
non-operating room anesthesia