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Preoperative Chewing Gum and Postoperative Nausea and Vomiting

Study on the Impact of Preoperative Chewing Gum on Postoperative Nausea and Vomiting in Robotic Surgery

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06446583
Enrollment
92
Registered
2024-06-06
Start date
2024-06-01
Completion date
2024-12-31
Last updated
2024-06-06

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

Conditions

Gynecologic Disease

Brief summary

General anesthesia for surgery can often lead to postoperative nausea and vomiting (PONV). Additionally, decreased or paralyzed bowel movements are among the most common complications following abdominal surgery, causing pain, abdominal distension, nausea, and vomiting, which can delay patient recovery and extend hospital stays. Therefore, meticulous perioperative management is crucial. In recent years, efforts have been made to reduce the burden of surgery, decrease postoperative complications, and promote rapid rehabilitation for a quicker return to daily life. These efforts also aim to reduce healthcare costs by shortening hospital stays and optimizing resources. Various interventions, such as early feeding, early removal of nasogastric tubes, and physical therapy, have been trialed in clinical settings to prevent prolonged bowel inactivity and paralysis. However, due to limited clinical efficacy, these methods are not routinely used. Recently, many researchers have reported the benefits of chewing gum in enhancing bowel motility and reducing PONV. However, there is limited research on the impact of chewing gum on PONV in robotic surgeries, which are considered less invasive compared to open or laparoscopic surgeries. Furthermore, there is particularly scarce research on the effects of preoperative gum chewing.

Interventions

OTHERChewing sugar-free gum

Upon arrival at the preoperative preparation room, patients begin chewing sugar-free gum provided by the preoperative nurse. They continue chewing until they enter the operating room (for at least 15 minutes). Before entering the operating room, it is confirmed that the gum has been discarded.

Sponsors

Min Suk Chae
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
19 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. Adult patients aged 19 to under 70 years 2. Scheduled elective robotic surgery 3. American Society of Anesthesiologists (ASA) Physical Status Classification I or II

Exclusion criteria

1. Cases where robotic surgery was planned but suddenly converted to another type of surgery 2. Patients with a history of dental damage, dentures, loose or capped teeth, or other unstable dental conditions 3. Patients with a history of temporomandibular joint (TMJ) damage or surgery 4. Head and neck surgeries 5. Emergency surgeries 6. Refusal to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
nausea and vomitingOne hour after surgery, referring to the period spent in the post-anesthesia care unitIncidence of nausea and vomiting in the post-anesthesia care unit

Contacts

Primary ContactMin Suk Chae, MD, PhD
shscms@catholic.ac.kr0222586150

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026