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Fasting Durations Before Bronchoscopy And The Discomfort Levels Of Patients

Association Between Different Fasting Durations Before Bronchoscopy And The Discomfort Levels Of Patients Around The Procedure

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06779084
Enrollment
84
Registered
2025-01-16
Start date
2025-01-31
Completion date
2026-12-31
Last updated
2025-01-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchoscopy, Fasting ( 6H for Solid ; 2H for Clear Fluid )

Brief summary

The goal of this clinical trial is to learn if patients feel more comfortable while being placed on contemporary fasting principle than on conventional fasting time during flexible bronchoscopy. The main questions it aims to answer are: To compare the thirty levels between patients with conventional fasting time (≥ 8 hours) and those with contemporary fasting principle (clear fluids for up to 2 hours before anesthesia) during flexible bronchoscopy To compare the levels of mucosal dryness between two groups of patients during flexible bronchoscopy To compare the levels of hunger between two groups of patients during flexible bronchoscopy To compare the levels of tiredness between two groups of patients during flexible bronchoscopy To compare the levels of fatigue between two groups of patients during flexible bronchoscopy To compare the levels of nausea/vomiting between two groups of patients during flexible bronchoscopy Participants will: Being placed on fasting either using conventional fasting time (≥ 8 hours) or with contemporary fasting principle (clear fluids for up to 2 hours before anesthesia) Being asked to respond to questions regarding thirsty, mucosal dryness, hunger, tiredness, fatigue, and nausea/vomiting in a visual analogue scale of 0 to 10

Interventions

OTHERcontemporary fasting principle

(clear fluids for up to 2 hours before anesthesia)

OTHERconventional fasting time

(≥ 8 hours)

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* planned flexible bronchoscopy

Exclusion criteria

* tracheostomy or intubated * known to be pregnant * significant functional or structural abnormalities of the gastrointestinal tract * oral intake prohibited and infeasible

Design outcomes

Primary

MeasureTime frameDescription
patient thirty levelright before the bronchoscopy procedureusing a visual analogue scale of 0 to 10

Secondary

MeasureTime frameDescription
patient hungerright before the bronchoscopy procedureusing a visual analogue scale of 0 to 10
patient tirednessright before the bronchoscopy procedureusing a visual analogue scale of 0 to 10
patient mucosal drynessright before the bronchoscopy procedureusing a visual analogue scale of 0 to 10
patient nausearight after the bronchoscopy procedureusing a visual analogue scale of 0 to 10
patient vomitingright after the bronchoscopy procedureabsent or present
patient fatigueright before the bronchoscopy procedureusing a visual analogue scale of 0 to 10

Contacts

Primary ContactChao-Chi Ho
ccho1203@ntu.edu.tw+886-2-23562905

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026