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Fasting Durations Before Bronchoscopy And The Discomfort Levels Of Patients

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National Taiwan University

Status

Not yet enrolling

Conditions

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

Treatments

Other: contemporary fasting principle
Other: conventional fasting time

Study type

Interventional

Funder types

Other

Identifiers

NCT06779084
202412025RINA

Details and patient eligibility

About

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

Enrollment

84 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

84 participants in 2 patient groups

contemporary fasting principle
Experimental group
Treatment:
Other: contemporary fasting principle
conventional fasting time
Active Comparator group
Treatment:
Other: conventional fasting time

Trial contacts and locations

0

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Central trial contact

Chao-Chi Ho

Data sourced from clinicaltrials.gov

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