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Clinical Trials/NCT01549353
NCT01549353
Completed
Not Applicable

Does Gum Chewing After Gynecologic Laparoscopy Stimulate Earlier Return of Bowel Motility?

Klinikum Klagenfurt am Wörthersee1 site in 1 country200 target enrollmentJuly 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Care
Sponsor
Klinikum Klagenfurt am Wörthersee
Enrollment
200
Locations
1
Primary Endpoint
Time to return to active bowel movements
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

Gum chewing has been reported to stimulate bowel motility after open surgery, such as cesarean section and other abdominal surgeries. In general, after laparoscopic surgery problems with reduced bowel motility are not as common as after open surgery. In this study the investigators test the hypothesis that gum chewing is enhancing rapid return of bowel motility after gynecologic laparoscopic surgery. Further the investigators study patient satisfaction and potential side effects of postoperative gum chewing.

Registry
clinicaltrials.gov
Start Date
July 2011
End Date
September 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Husslein Heinrich, MD

Principal investigator

Klinikum Klagenfurt am Wörthersee

Eligibility Criteria

Inclusion Criteria

  • all gynecologic laparoscopic surgery
  • normal level of CA 125 postmenopausal

Exclusion Criteria

  • loose teeth
  • chronic obstipation
  • laparotomy
  • operations longer then 3 h

Outcomes

Primary Outcomes

Time to return to active bowel movements

Time Frame: participants will be followed for the duration of hospital stay

First active bowel movement is defined as time from operation until first passage of flatus. Time until first defecation will also be measured.

Secondary Outcomes

  • patient satisfaction with postoperative gum chewing(participants will be followed for the duration of the hospital stay)
  • Number of participants with adverse events(participants will be followed for the duration of hospital stay)

Study Sites (1)

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