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NCT Number: NCT06779084

Fasting Durations Before Bronchoscopy And The Discomfort Levels Of Patients

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

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

contemporary fasting principle

Other

(clear fluids for up to 2 hours before anesthesia)

conventional fasting time

Other

(≥ 8 hours)

Primary outcomes

  1. patient thirty level

    Time frame: right before the bronchoscopy procedure

    using a visual analogue scale of 0 to 10

Secondary outcomes

  1. patient mucosal dryness

    Time frame: right before the bronchoscopy procedure

    using a visual analogue scale of 0 to 10

  2. patient hunger

    Time frame: right before the bronchoscopy procedure

    using a visual analogue scale of 0 to 10

  3. patient tiredness

    Time frame: right before the bronchoscopy procedure

    using a visual analogue scale of 0 to 10

  4. patient fatigue

    Time frame: right before the bronchoscopy procedure

    using a visual analogue scale of 0 to 10

  5. patient nausea

    Time frame: right after the bronchoscopy procedure

    using a visual analogue scale of 0 to 10

  6. patient vomiting

    Time frame: right after the bronchoscopy procedure

    absent or present

Study contacts

Contact information is provided by the study sponsor or research team.

Chao-Chi Ho

CONTACT

[email protected]

+886-2-23562905

Sponsors and collaborators

Lead sponsor

National Taiwan University Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jan 16, 2025
Registry last updated
Jan 16, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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