CClinicalTrials.gg
CompletedNCT07796529Updated Sep 1, 2026

Menthol Chewing Gum After Laparoscopic Colorectal Surgery

An interventional study of Menthol Chewing Gum in Postoperative Nausea and Vomiting, Bowel Functions and Postoperative Recovery, sponsored by Sennur Kula Şahin. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-01.

Sponsored by Sennur Kula Şahin · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

This randomized controlled trial was conducted to evaluate the effect of menthol chewing gum on postoperative nausea and vomiting, bowel function, and recovery in patients undergoing laparoscopic colorectal surgery. A total of 50 patients were randomly assigned to an intervention group (n=25) or a control group (n=25). Participants in the intervention group received menthol chewing gum in addition to standard postoperative care, while participants in the control group received standard postoperative care only. Nausea, bowel function, and postoperative recovery were assessed during the first three postoperative days.

Read the detailed description

Postoperative nausea and vomiting and delayed return of bowel function are common concerns following laparoscopic colorectal surgery and may affect postoperative recovery. Chewing gum is a non-pharmacological intervention that may stimulate gastrointestinal activity.

This randomized controlled trial evaluated the effect of menthol chewing gum on postoperative nausea and vomiting, bowel function, and recovery in patients undergoing laparoscopic colorectal surgery. Participants were randomly allocated to an intervention group or a control group.

Both groups received routine postoperative treatment and nursing care. In the intervention group, participants chewed menthol gum for 30 minutes and repeated the intervention three hours later. The same procedure was applied on the first, second, and third postoperative days. Participants in the control group received routine postoperative treatment and care without menthol chewing gum.

Postoperative nausea, bowel function, and recovery status were evaluated during the first three postoperative days. Postoperative recovery was assessed using the Surgical Recovery Status Scale, and nausea intensity was assessed using a Visual Analog Scale.

02

Conditions studied

  • Postoperative Nausea and Vomiting
  • Bowel Functions
  • Postoperative Recovery

Keywords

  • Menthol Chewing Gum
  • Chewing Gum
  • Laparoscopic Colorectal Surgery
  • Postoperative Nausea and Vomiting
  • Bowel Function
  • Surgical Recovery
  • Nonpharmacological Intervention
03

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Aged 18-60 years
  • Willing to participate in the study
  • At least literate
  • Able to communicate without cognitive, sensory, or verbal impairment
  • No diagnosed psychiatric disorder
  • No vertigo
  • Undergoing elective surgery
  • Not using sedative, anxiolytic, or similar medications
  • Able to speak Turkish
  • Able to chew gum
  • No allergy to menthol or mint
  • No history of jaw or oral surgery

Exclusion criteria

Exclusion Criteria:

  • Absence of teeth
  • Unwilling to chew gum
04

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Care provider)
Enrollment
50 participants (actual)

Study arms

  • Experimental
    1

    Menthol Chewing Gum Group

    Behavioral: Menthol Chewing Gum

  • No intervention
    2

    Control Group

Interventions

  • BehavioralMenthol Chewing Gum

    Participants chewed menthol gum for 30 minutes, followed by a second 30-minute chewing session three hours later. This intervention was repeated on postoperative days 1, 2, and 3 in addition to standard postoperative care.

05

What researchers measure

Primary outcomes

  1. Postoperative Nausea and Vomiting Frequency

    The frequency of postoperative nausea and vomiting was recorded for each participant during the first three postoperative days. Higher values indicate a greater frequency of nausea and vomiting.

    Time frame: Postoperative days 1, 2, and 3

Secondary outcomes

  1. Postoperative Gas Passage Frequency

    The frequency of defecation was recorded during the first three postoperative days as an indicator of postoperative bowel function.

    Time frame: Postoperative days 1, 2, and 3

Other outcomes

  1. Postoperative Defecation Frequency

    The frequency of defecation was recorded during the first three postoperative days as an indicator of postoperative bowel function.

    Time frame: [Time Frame: Postoperative days 1, 2, and 3]

  2. Postoperative Recovery Status

    Postoperative recovery was assessed using the Surgical Recovery Status Scale. The scale consists of 25 items and five subscales: psychological symptoms, physical activities, general symptoms, bowel symptoms, and desire-related symptoms. Item scores are averaged to obtain the total score. Higher scores indicate greater difficulty in postoperative recovery, whereas lower scores indicate easier recovery.

    Time frame: Postoperative days 1, 2, and 3

06

Study locations

1 site
  • Istinye University Medical Park Gaziosmanpasa Hospital
    Istanbul, Istanbul 34010, Turkey (Türkiye)
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07796529
Lead sponsor
Sennur Kula Şahin
Responsible party
Sennur Kula Şahin (Assoc.Prof, Istinye University) — Sponsor-investigator
First posted
Sep 1, 2026
Start date
Jan 15, 2024
Primary completion
Apr 25, 2024
Completion
Apr 25, 2024
Last update
Sep 1, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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