Chewing Gum and Cold Gargle on Post-Bronchoscopy Symptoms
The Effect of Chewing Gum and Gargling With Cold Water on Post-Bronchoscopy Sore Throat, Dysphagia, and Patient Satisfaction: A Randomized Controlled Study
1 other identifier
interventional
100
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 10, 2025
CompletedFirst Submitted
Initial submission to the registry
April 2, 2026
CompletedFirst Posted
Study publicly available on registry
April 8, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 11, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 11, 2026
CompletedApril 13, 2026
April 1, 2026
6 months
April 2, 2026
April 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Severity of Post-Bronchoscopy Sore Throat
Sore throat severity will be measured using a Visual Analog Scale (VAS), where 0 represents 'no pain' and 10 represents 'the most severe pain imaginable.' Higher scores indicate greater pain severity.
Baseline (pre-procedure), 2nd hour, and 24th hour post-procedure.
Secondary Outcomes (2)
Severity of Post-Bronchoscopy Dysphagia
Baseline (pre-procedure), 2nd hour, and 24th hour post-procedure.
Patient Satisfaction Level
2nd hour and 24th hour post-procedure.
Study Arms (3)
Chewing Gum Group
EXPERIMENTALPatients in this group will chew sugar-free xylitol gum for 15 minutes immediately before bronchoscopy.
Cold Water Gargle Group
EXPERIMENTALPatients in this group will gargle with cold water (8-12°C) twice for 30 seconds each, 15 minutes before bronchoscopy.
Control Group
NO INTERVENTIONPatients in this group will receive standard care without additional interventions.
Interventions
Patients will gargle with cold water (8-12°C) twice for 30 seconds each, 15 minutes before the bronchoscopy procedure.
Patients will chew sugar-free xylitol gum for 15 minutes immediately before the bronchoscopy procedure
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Gulhane Training and Research Hospital
Ankara, 06010, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
neriman yükseltürk şimşek
ankara u
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- Patients are blinded to their group assignment and study hypotheses. Researchers administering the interventions are not blinded.
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
April 2, 2026
First Posted
April 8, 2026
Study Start
November 10, 2025
Primary Completion
May 11, 2026
Study Completion
May 11, 2026
Last Updated
April 13, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared to protect participant privacy and confidentiality.