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Completed

NCT Number: NCT06952985

Role of Gum Chewing in Post-operative Gut Motility After Cesarean Section

Many women deliver by caesarean section nowadays. The proportion of women who deliver by caesarean section ranges from 15% to over 50%, in some countries. After a caesarean section it is common for the bowel to stop working for several hours or days. Although this usually resolves by itself in a few days, it may be very uncomfortable. The retained gases and stools can cause the mother's belly to become swollen and painful with cramps and she may feel nauseated and vomit so she is not able to eat. She may need additional medications to ease these symptoms and her hospital discharge may be delayed. The use of medications that relieve pain during labour and painkillers following the surgery can also delay bowel function. Small intestine activity after abdominal operations returns to normal function within a few hours, gastric activity returns to normal within 24-48 hours, and colon activity returns to normal within 48-72 hours. Due to the delayed motility of the gastrointestinal system in the postoperative period, gas and secretions accumulate in the stomach and small and large intestines, which causes abdominal distension, nausea, vomiting, and pain, all of which negatively affect the comfort level of the patients. Chewing sugar-free gum after cesarean section can promote the early recovery of gastrointestinal function, but the side effects of chewing gum are still unclear, which needs more clinical, large sample and high-quality studies to further verify.

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Key information

Age range

18 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

CMH Gujranwala

Gujranwala, Punjab Province, 52230, Pakistan

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Females of age 18-40 years
  • Parity <5
  • Presenting at gestational age ≥ 37 weeks,
  • Undergoing cesarean section (as per operational definition) under spinal anesthesia

Exclusion criteria

  • Females with history of chronic constipation (medical record)
  • Females with obstructed labour, hypothyroidism (TSH>5IU)
  • Females with intra operative complications such as bowel injury, history of gastrointestinal surgery, and water and electrolyte disturbances (on medical record), abnormal placenta (accrete, increta, previa, abruption)

Treatment and study plan

Sugar free chew gum

Dietary Supplement

Chew gum has a role in ERAS protocol which is significant in early post operative recovery as compared to normal routine care methods

Nil Per Oral

Other

According to classic protocols patient were kept nil per oral till bowel sounds were audible

Primary outcomes

  1. Mean Time of Passage of First flatus

    Time frame: 06 Months

    In group A, females were given chewing gum 6 hours after the surgery, three times a day till passage of flatus. In group B, females were managed as per standard routine protocol i.e. allowing oral when bowel sounds are audible. Mean time of passage of first flatus since procedure was noted in terms of hours.

Secondary outcomes

  1. Mean Duration of Hospital Stay

    Time frame: 06 Months

    In both groups mean duration of hospital stay was noted in terms number of days required to stay in the hospital after cesarean. Patients were discharged once they were pain free and on oral medication.

Sponsors and collaborators

Lead sponsor

Dr Maryam Aslam

Other

Collaborators

  • CMH Gujranwala

Registry information

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
May 1, 2025
Registry last updated
May 1, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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