Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07517926

Chewing Gum and Cold Gargle on Post-Bronchoscopy Symptoms

Led by Ankara University · Updated on 2026-04-13

100

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to evaluate the effects of chewing gum and gargling with cold water on common post-bronchoscopy symptoms, such as sore throat and difficulty swallowing (dysphagia). Bronchoscopy is a procedure that can cause temporary throat discomfort. In this randomized controlled trial, patients will be divided into groups to receive either chewing gum, cold water gargle, or standard care. The researchers will then measure and compare patient satisfaction levels and the severity of throat symptoms to determine if these simple interventions can improve patient comfort after the procedure.

CONDITIONS

Official Title

Chewing Gum and Cold Gargle on Post-Bronchoscopy Symptoms

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Being 18 years of age or older
  • Having a scheduled diagnostic bronchoscopy
  • Having normal speech and swallowing functions
  • Being conscious and able to communicate
  • Volunteering to participate in the study
Not Eligible

You will not qualify if you...

  • Complications during bronchoscopy
  • Gastroesophageal reflux
  • Use of non-steroidal anti-inflammatory drugs
  • Receiving steroid treatment within 1 week prior to the procedure
  • Active infection or disease in the mouth or throat area
  • History of allergy or intolerance to the procedure
  • Previous anatomical or functional impediment to chewing gum or gargling

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Gulhane Training and Research Hospital

Ankara, Turkey (Türkiye), 06010

Actively Recruiting

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Research Team

N

Neriman Yükseltürk Şimşek, PHD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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