The Effect of Gum Chewing on Postoperative Ileus After Gynecologic Surgery
Completed · Phase 1/Phase 2
Conditions studied: Postoperative Ileus
In brief
The investigators are randomizing patients to receive chewing gum (Extra Sugar Free, Spearment) every 4 hours during waking hours for 15 minutes versus standard postoperative care. The investigators then have them fill out a survey in house and 1 week after their surgery that record time to first flatus, hunger, toleration of clear liquids and food and some information about pain, satisfaction, and quality of life. The investigators contact them via phone and email a maximum of three times in order to collect this information. 30 days postoperatively the investigators also contact them and perform a chart review for any postoperative complications.
Key facts
- Study ID
- NCT01579175
- Run by
- Johns Hopkins University
- People needed
- 294
- Starts
- 2010-01-01
- Expected to finish
- 2013-02-01
- Last updated by the study team
- 2013-03-14
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- 18 years or older
- Undergoing benign gynecologic surgery via an exploratory laparotomy
- Capable of giving consent
You may not qualify if…
- Oromaxillary or mental disturbances that would make chewing gum dangerous with regards to mastication or aspiration
- Intubated or unconscious when leaving the OR
- Bowel resection performed at the time of surgery
- Active bowel disease (IBD, appendicitis, etc)
- Gynecologic malignancy
Where it is running
- Johns Hopkins Bayview — Baltimore, Maryland, United States
- Johns Hopkins Hospital — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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