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The Effects of Chewing Gum on Postoperative Nausea and Vomiting.

A Pilot Randomized Controlled Study on The Effects of Chewing Gum on Postoperative Nausea and Vomiting in Critically Ill Patients

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12617001185358
Acronym
The ECG PONV Study
Enrollment
90
Registered
2017-08-11
Start date
2017-10-18
Completion date
2019-01-31
Last updated
2020-12-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Postoperative nausea and vomiting (PONV) is a common complication that may cause significant morbidity. It is usually treated with anti-emetics. Recently, Chewing Gum (GC) showed similar level of efficacy to ondansetron in a pilot controlled trial of surgical patients. Moreover, CG has bee shown to reduce postoperative gut malfunction and vomiting after colorectal surgery However, to date, CG has not bee studied in the prevention of PONV in patients admitted to the intensive care unit (ICU). Thus we aim to perform a study to evaluate the comparative effect of CG compared with the effects of taking a 20 ml sip of water in the prevention of PONV in patients admitted to the ICU after major surgery. Patients will be randomly allocated to be given sugarless plain CG or a 20 ml sip of water 4 hourly for 24 hours. The nurse looking after the patient will record the effects of the intervention on the presence of nausea, its duration, and severity using a visual analogue scale every 4 hours. The number of episodes of vomiting and retching will be recorded. Rescue anti-emetic therapy if the nausea is rated > 5, or if vomiting has occurred. Nausea and vomiting assessments will be made 30 minutes after the patient had been given rescue medication. If the CG intervention proves effective, it will represent an important and easily deployed, safe step towards making the patient's post-operative period less distressing.

Interventions

Chewing mint flavoured gum four-hourly for up to 15 minutes during first 24 postoperative hours. Data will be collected if the intervention was given or not and the reason why it wasn't given if not.

Sponsors

Austin Health
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Admission to Austin Hospital ICU Age 18 year of greater Immediate (Within 12 hours) post-operative period An anticipated ICU length of stay of > 12 hours after randomization.

Exclusion criteria

Ongoing mechanical ventilation with endotracheal tube. Inability to chew due to presence of dentures Inability to chew due to oropharngeal or maxillary surgery Admission after oesophageal surgery Recent Extubation < 1 hours Dysphagia

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 25, 2026