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Effect of Chewing Gum on Post-operative Ileus (GUMPI)

Does Chewing Gum Affect the Incidence of Post-operative Ileus in Patients Undergoing Spine Surgery?

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02847364
Acronym
GUMPI
Enrollment
100
Registered
2016-07-28
Start date
2016-02-29
Completion date
2023-12-31
Last updated
2022-02-17

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

Conditions

Ileus

Keywords

chewing gum, prevention

Brief summary

The purpose of this study is to determine whether chewing gum post-operatively decreases the time to first flatus or defecation in patients undergoing spine surgery as a indirect indicator of post-operative ileus.

Detailed description

The patients undergoing spine surgery are at risk of developing post-operative ileus, which will lengthen the hospital stay and cause gastrointestinal distress in patients. Post-operative sham feeding in form of chewing a gum seems to increase the functionality of gastro-intestinal tract earlier in patients who have undergone gastro-intestinal and gynecological surgeries. This study will recruit patients undergoing spine surgery at the investigators medical center and allocate them randomly into two equal groups. Patients in one group will be asked to chew gum after surgery and the other group will not be offered anything on chew on. Both groups will be kept nothing per os (NPO) otherwise till the first bowel movement. The first post-operative flatus and defecation time will be recorded as primary measures and other main outcomes will include first post-operative meal, length of stay and presence of ileus. The descriptive parameters of the two groups will also be recorded as related to relevant medical history, surgery, and post-operative care, to adjust for its effect on outcome measures. This study will identify any beneficial effect that chewing gum will have on post-operative ileus development and might be helpful in establishing better post-operative care protocols in patients undergoing spine surgery.

Interventions

DIETARY_SUPPLEMENTchewing gum

The patient will chew one piece (1.45g) of regular chewing gum starting morning of post-operative day 1 for 30 minutes each time, three times per day, till the first bowel movement.

Sponsors

American University of Beirut Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
13 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient 13 years of age or older * Patients who will undergo spine decompression, laminectomy (cervical, lumbar and/or thoracic), discectomy, foraminotomy, or corpectomy, with or without arthrodesis, with or without instrumentation.

Exclusion criteria

* Less than 13 years of age * Patients who have undergone with abdominal surgery within the last month * Patients with inability or problems with chewing and/or dysphagia * Patients who are expected to be kept intubated after surgery * Patients who are allergic to any chewing gum component

Design outcomes

Primary

MeasureTime frameDescription
first defecation timepost-operative hospital stay till discharge (up to 5 days)time of passing the first defecation after surgery, monitored for first defecation for up to 5 days after surgery.
first flatus timepost-operative hospital stay till discharge (up to 5 days)time of passing the first flatus after surgery; monitored for first flatus for up to 5 days after surgery.

Secondary

MeasureTime frameDescription
LOShospital stay (average of 5 days)the length of hospital stay (throughout their hospital stay, average of 5 days)
Meal timepost-operative hospital stay till discharge (up to 5 days)The time of first tolerable meal after surgery; monitored for first tolerable meal for up to 5 days after surgery.
post-operative ileuspost-operative hospital stay till discharge (up to 5 days)presence of post-operative ileus; monitored for ileus for up to 5 days after surgery.

Countries

Lebanon

Contacts

Primary ContactAsdghig Der-Boghossian, LD, MS
ahd14@mail.aub.edu+961-1-350000

Outcome results

None listed

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