Fasting Durations Before Bronchoscopy And The Discomfort Levels Of Patients
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: contemporary fasting principle, conventional fasting time.
- Who it may be relevant to
- Registry conditions: Bronchoscopy, Fasting ( 6H for Solid ; 2H for Clear Fluid ). Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Association Between Different Fasting Durations Before Bronchoscopy And The Discomfort Levels Of Patients Around The Procedure
Overview
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
- Other contemporary fasting principle
(clear fluids for up to 2 hours before anesthesia) - Other conventional fasting time
(≥ 8 hours)
Primary outcome measures
- patient thirty level [Time frame: right before the bronchoscopy procedure]
Secondary outcome measures (6)
- patient mucosal dryness [Time frame: right before the bronchoscopy procedure]
- patient hunger [Time frame: right before the bronchoscopy procedure]
- patient tiredness [Time frame: right before the bronchoscopy procedure]
- patient fatigue [Time frame: right before the bronchoscopy procedure]
- patient nausea [Time frame: right after the bronchoscopy procedure]
- patient vomiting [Time frame: right after the bronchoscopy procedure]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Other
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06779084 · 202412025RINA