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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01131416
Other study ID # 10FEB010938
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received May 25, 2010
Last updated June 27, 2011
Start date May 2010
Est. completion date June 2011

Study information

Verified date June 2011
Source Chiang Mai University
Contact n/a
Is FDA regulated No
Health authority Thailand: Ethical Committee
Study type Interventional

Clinical Trial Summary

Following all abdominal surgery, paralytic ileus commonly develops. Surgeons have traditionally withheld postoperative oral intake until the return of bowel function to prevent related complications. Gum chewing can stimulates bowel movement and promotes the return of bowel function through the cephalic-vagal reflex and increased intestinal enzymes secretion.

The objectives of this study are to examine effects of adding gum chewing to the conventional postoperative feeding regimen on the return of bowel function, its related complications, and patients' satisfaction.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date June 2011
Est. primary completion date June 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 15 Years to 50 Years
Eligibility Inclusion Criteria:

- Pregnant women undergoing cesarean delivery

Exclusion Criteria:

- Perioperative hyperalimentation

- Recent chemotherapy

- Concurrent bowel surgery

- Previous bowel surgery

- Concurrent bowel obstruction

- History of inflammatory bowel diseases

- Previous abdominal/pelvic radiation

- Postoperative placement of endotracheal tube/nasogastric tube

- Postoperative admission to intensive care unit

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Gum chewing
Gum chewing (30 minutes in duration each time, 4 times/days at the usual time of meal, until the first flatus) in addition to conventional postoperative feeding schedule

Locations

Country Name City State
Thailand Faculty of Medicine, Chiang Mai University Chiang Mai

Sponsors (1)

Lead Sponsor Collaborator
Chiang Mai University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative interval until the first flatus Up to 7 days after delivery No
Secondary Postoperative interval until the first passage of stool Up to 7 days after delivery No
Secondary Clinically significant postoperative ileus Up to 7 days after delivery No
Secondary Postoperative hospital stay Up to 7 days after delivery Yes
Secondary Related complications Up to 7 days after delivery Yes
Secondary Patients' satisfaction Up to 7 days after delivery No
See also
  Status Clinical Trial Phase
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Completed NCT03884244 - Postoperative Chewing Gum and Gynecological Laparoscopic Surgery N/A
Withdrawn NCT01389986 - Effects of Gum Chewing on Recovery of Bowel Function Following Abdominal Surgery for Endometrial and Ovarian Cancer Phase 2/Phase 3
Recruiting NCT04190173 - Efficacy of PRUcalopride in Critically Ill Patients With Paralytic ILeus Phase 3
Completed NCT06113718 - The Impact of Preoperative Bowel Exercise on Postoperative Bowel Functions in Gynecologic Malignancies N/A
Recruiting NCT03041675 - Effects of Laser Acupuncture Therapy on Paralytic Ileus N/A
Active, not recruiting NCT01607307 - Daikenchuto for Intestinal Dysmotility and Prevention of Postoperative Paralytic Ielus After Pancreaticoduodenectomy Phase 2