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NCT Number: NCT07517926

Chewing Gum and Cold Gargle on Post-Bronchoscopy Symptoms

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Gulhane Training and Research Hospital

Ankara, 06010, Turkey (Türkiye)

Location status: Recruiting

Location contact

Ferdağ Bölükbaş, PHD

SUB_INVESTIGATOR

Neriman Yükseltürk Şimşek, PHD

CONTACT

[email protected]

03123042242

yakup aslan, md

SUB_INVESTIGATOR

About this study

Study Implementation and Procedures

All patients in the intervention and control groups will be informed about the study's purpose. Patients undergoing bronchoscopy receive routine verbal education from bronchoscopy nurses. In addition to routine education, the intervention groups will receive specific instructions from the researchers. Patients will be blinded to their randomization status and study hypotheses. However, researchers will not be blinded as they will perform the interventions. The chewing gum and cold water gargle procedures will be explained and demonstrated to the intervention groups during face-to-face interviews.

Chewing Gum Procedure All patients will follow the hospital's standard pre-procedure fasting protocol (8 hours of fasting). A researcher will be responsible for supervising the chewing gum procedure. Patients in this group will be asked to chew a commercially available sugar-free gum containing xylitol for 15 minutes immediately before the procedure. After 15 minutes of chewing, patients will discard the gum. The researcher will ensure the gum is removed before the patient is admitted for bronchoscopy. Patients will be strictly instructed not to swallow the gum.

Cold Water Gargle Procedure Patients in this group will perform a cold water gargle under the supervision of a researcher 15 minutes before the procedure. Patients will be instructed not to swallow the water. The researcher will prepare the water at a temperature between 8-12°C (refrigerator coldness). Patients will gargle twice for 30 seconds each, approximately 15 minutes before the procedure.

Control Group The control group will receive standard hospital procedures without any additional intervention.

Data Collection and Evaluation Sore throat, difficulty swallowing (dysphagia), and patient satisfaction levels will be evaluated before the procedure, and at the 2nd and 24th hours post-procedure. The 24-hour evaluation will be conducted via telephone by the research team.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • • 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

Exclusion criteria

  • • 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

Treatment and study plan

Chewing Gum

Behavioral

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

Cold Water Gargle

Behavioral

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

Primary outcomes

  1. Severity of Post-Bronchoscopy Sore Throat

    Time frame: Baseline (pre-procedure), 2nd hour, and 24th hour post-procedure.

    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.

Secondary outcomes

  1. Severity of Post-Bronchoscopy Dysphagia

    Time frame: Baseline (pre-procedure), 2nd hour, and 24th hour post-procedure.

    Dysphagia severity will be measured using a Visual Analog Scale (VAS), where 0 represents "no difficulty swallowing" and 10 represents "extreme difficulty swallowing." Higher scores indicate greater difficulty swallowing

  2. Patient Satisfaction Level

    Time frame: 2nd hour and 24th hour post-procedure.

    Patient satisfaction with the procedure and post-operative comfort will be measured using a satisfaction scale (e.g., 0-10 scale or a specific survey). Higher scores indicate higher satisfaction levels.

Study contacts

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

Neriman Yükseltürk Şimşek, PHD

CONTACT

[email protected]

0312 3042242

Sponsors and collaborators

Lead sponsor

Ankara University

Other

Registry information

Official study title

The Effect of Chewing Gum and Gargling With Cold Water on Post-Bronchoscopy Sore Throat, Dysphagia, and Patient Satisfaction: A Randomized Controlled Study

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Apr 8, 2026
Registry last updated
Apr 13, 2026

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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