Fasting Durations Before Bronchoscopy And The Discomfort Levels Of Patients
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNational Taiwan University Hospital
About this trial
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
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
planned flexible bronchoscopy
Disqualifiers
tracheostomy or intubated
known to be pregnant
significant functional or structural abnormalities of the gastrointestinal tract
oral intake prohibited and infeasible
Trial design
Design model
Parallel
Treatments tested in this trial
contemporary fasting principle
Other intervention(clear fluids for up to 2 hours before anesthesia)
conventional fasting time
Other intervention(≥ 8 hours)
Treatment groups
84 Participants
are divided into 2 treatment groupsGroup A: contemporary fasting principleExperimental treatment 1 intervention
Group B: conventional fasting timeActive comparator 1 intervention
Trial outcomes
Primary outcomes
1
patient thirty level
using a visual analogue scale of 0 to 10
Time frame
right before the bronchoscopy procedureSecondary outcomes
1
patient mucosal dryness
using a visual analogue scale of 0 to 10
Time frame
right before the bronchoscopy procedure2
patient hunger
using a visual analogue scale of 0 to 10
Time frame
right before the bronchoscopy procedure3
patient tiredness
using a visual analogue scale of 0 to 10
Time frame
right before the bronchoscopy procedure4
patient fatigue
using a visual analogue scale of 0 to 10
Time frame
right before the bronchoscopy procedureLocations
Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: