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

Sponsor
American University of Beirut Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT02847364
Collaborator
(none)
100
1
2
94
1.1

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: chewing gum
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Does Chewing Gum Affect the Incidence of Post-operative Ileus in Patients Undergoing Spine Surgery?
Study Start Date :
Feb 1, 2016
Anticipated Primary Completion Date :
Feb 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Chewing gum group

The patients will be asked to chew on a regular chewing gum starting morning of post-operative day 1 until the first bowel movement.

Dietary Supplement: chewing 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.

No Intervention: Control group

These patients will not be offered any food/beverage orally. Patients will be asked not to eat or chew anything till the first bowel movement.

Outcome Measures

Primary Outcome Measures

  1. first flatus time [post-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.

  2. first defecation time [post-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.

Secondary Outcome Measures

  1. LOS [hospital stay (average of 5 days)]

    the length of hospital stay (throughout their hospital stay, average of 5 days)

  2. Meal time [post-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.

  3. post-operative ileus [post-operative hospital stay till discharge (up to 5 days)]

    presence of post-operative ileus; monitored for ileus for up to 5 days after surgery.

Eligibility Criteria

Criteria

Ages Eligible for Study:
13 Years and Older
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 American University of Beirut Medical Center Beirut Lebanon 11-236

Sponsors and Collaborators

  • American University of Beirut Medical Center

Investigators

  • Principal Investigator: Abdel Majid Sheikh Taha, MD, American University of Beirut Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Dr. Abdel Majid Sheikh Taha, Clinical Instructor of Orthopedic Surgery, American University of Beirut Medical Center
ClinicalTrials.gov Identifier:
NCT02847364
Other Study ID Numbers:
  • SUR.AMST.01
First Posted:
Jul 28, 2016
Last Update Posted:
Feb 17, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Dr. Abdel Majid Sheikh Taha, Clinical Instructor of Orthopedic Surgery, American University of Beirut Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 17, 2022