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The Effect of Gum Chewing on Bowel Function After Cesarean Section

S

Sisli Hamidiye Etfal Training and Research Hospital

Status

Completed

Conditions

Splinter of Gum

Treatments

Other: chew gum

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This study is a randomised controlled trial that included 150 pregnant women undergoing cesarean in Sisli Ethal Training and Research Hospital, Department of Obstetrics and Gynecology, Istanbul, Turkey. It was carried out in the period from October 1, 2015 to December 31, 2015. After operation, the participants are going to randomly assigned into two groups by using cards. The patients are going to randomized into two groups by using a sealed enveloped system.The patients in the study group, will chew one sugar less gum for 30 minutes in postoperative 3., 5. and 7. hours. The control group will be followed without chew gum. All patients will note the time of first rumbling of the stomach, first feeling of hunger and the first gas outlet.

Full description

For elective cases, all participants are going to given nothing by mouth since midnight before surgery, and all operations are going to perform in the morning. For those who had emergency cesarean section, nothing is going to given per oral for at least 4 hours before the start of the operation. Operation data is going to recorded including surgical setting, type of cesarean section, previous surgery, adhesion and operation time.

After operation, the participants are going to randomly assigned into two groups by using cards. The patients are going to randomized into two groups by using a sealed enveloped system. A blue card and an orange card are going to sealed in separate envelopes. Blue card means patients will chewgum.

The patients in the study group, will chew one sugar less gum for 30 minutes in postoperative 3., 5. and 7. hours. The control group will be followed without chew gum. Both patient groups will be mobilized in postoperative 6 hour and 8 hour after the operation, juicy food will be given. It will be introduced to solid foods after bowel movements and gas output occurs. All patients postoperatively 4, 6, 8, 10, 12, 24 and 48 hours will be examined and bowel sounds will be oscult. Gas evolution is still not, enema will be applied. All patients will note the time of first rumbling of the stomach, first feeling of hunger and the first gas outlet.

Enrollment

150 patients

Sex

Female

Ages

18 to 44 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. pregnant women who is at least 18 years of age
  2. pregnant women whose body mass index is under 35
  3. pregnant women who is going to have cesarean section.

Exclusion criteria

  1. cesarean hysterectomy,
  2. surgical management of severe postpartum hemorrhage
  3. previous bowel surgery
  4. women with history of drug consumption,especially opioids
  5. water and electrolyte disturbances
  6. pancreatitis or peritonitis
  7. inability to chew gum
  8. diabetes, pregnancies accompanied by coagulopathy like pre-eclampsia, hypothyroidism, muscular and neurological disorders
  9. postoperative admission to intensive care unit
  10. history of abdominal surgery except cesarean section
  11. history of postoperative ileus
  12. patients with drains

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

150 participants in 2 patient groups, including a placebo group

postoperative chew gum
Active Comparator group
Description:
The patients in the study group will chew one sugarless gum for 30 minutes in postoperative 3., 5. and 7. hours.
Treatment:
Other: chew gum
without postoperative chew gum
Placebo Comparator group
Description:
The control group will be followed without chew gum.
Treatment:
Other: chew gum

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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