Clinical Trial

Preoperative Chewing Gum on Anxiety and Postoperative Nausea and Vomiting, Gastrointestinal Function

Active, Not Recruiting
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Record status
This record was last updated February 26, 2025 (before its estimated June 2025 completion). Its status may not reflect the trial's current state.
Summary
The aim of this study was to investigate the effects of chewing gum before surgery on preoperative anxiety, postoperative gastrointestinal functions (time to first gas, time to first defecation, bowel sounds, abdominal distension) and nausea and vomiting in patients undergoing abdominal surgery. Hypotheses of the Study: In patients undergoing abdominal surgery; H1.1: The first gas output time (hour) is shorter in patients who chew gum before surgery compared to patients who do not chew gum H1.2: The first defecation time (hour) is shorter in patients who chew gum before surgery compared to patients who do not chew gum H1.3: The bowel sounds are heard shorter in patients who chew gum before surgery compared to patients who do not chew gum H1.4: The abdominal distension rate is lower in patients who chew gum before surgery compared to patients who do not chew gum H1.5: The nausea and vomiting rate is lower in patients who chew gum before surgery compared to patients who do not chew gum H1.6: Preoperative anxiety levels of patients who chew gum before surgery are lower than those of patients who do not chew gum Preoperative intervention group patients will chew sugarless gum for at least 30 minutes 30-60 minutes before surgery. The gum will be removed before going to the operating room. No intervention will be performed on control group patients, and standard care will be applied.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-09-16.
Status change: Not Yet Recruiting → Active, Not Recruiting 2025-02-25
Trial Details
NCT Number NCT06603025
Lead Sponsor Eastern Mediterranean University
Conditions Gum Chewing, Preoperative, Anxiety, Postoperative Nausea and Vomiting
Enrollment 70 participants
Start Date 2024-09-06
Primary Completion 2025-06 (estimated)
Study Completion 2025-07 (estimated)
Updated on ClinicalTrials.gov 2025-02-26