NCT07517926

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

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Nov 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

April 2, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 8, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 11, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 11, 2026

Completed
Last Updated

April 13, 2026

Status Verified

April 1, 2026

Enrollment Period

6 months

First QC Date

April 2, 2026

Last Update Submit

April 7, 2026

Conditions

Keywords

BronchoscopySore ThroatDysphagiaChewing GumCold Water GargleNursing Care

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

EXPERIMENTAL

Patients in this group will chew sugar-free xylitol gum for 15 minutes immediately before bronchoscopy.

Behavioral: Chewing Gum

Cold Water Gargle Group

EXPERIMENTAL

Patients in this group will gargle with cold water (8-12°C) twice for 30 seconds each, 15 minutes before bronchoscopy.

Behavioral: Cold Water Gargle

Control Group

NO INTERVENTION

Patients 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.

Cold Water Gargle Group
Chewing GumBEHAVIORAL

Patients will chew sugar-free xylitol gum for 15 minutes immediately before the bronchoscopy procedure

Chewing Gum Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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)

RECRUITING

MeSH Terms

Conditions

PharyngitisDeglutition DisordersPatient Satisfaction

Interventions

Chewing Gum

Condition Hierarchy (Ancestors)

Respiratory Tract InfectionsInfectionsPharyngeal DiseasesStomatognathic DiseasesRespiratory Tract DiseasesOtorhinolaryngologic DiseasesEsophageal DiseasesGastrointestinal DiseasesDigestive System DiseasesTreatment Adherence and ComplianceHealth BehaviorBehavior

Intervention Hierarchy (Ancestors)

Plant GumsBiopolymersPolymersMacromolecular SubstancesPolysaccharidesCarbohydratesPlant ExudatesBiological ProductsComplex MixturesCandyFoodDiet, Food, and NutritionPhysiological PhenomenaFood and Beverages

Study Officials

  • neriman yükseltürk şimşek

    ankara u

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Neriman Yükseltürk Şimşek, PHD

CONTACT

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
Model Details: This is a three-arm, randomized, parallel-group study comparing two interventions (chewing gum and cold water gargle) with a standard care control group
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.

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