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Randomized Controlled Trial of Chewing Gum on Postoperative Patients' Gastrointestinal Function Recovery

Randomized Controlled Trial of Chewing Gum on Postoperative Patients' Gastrointestinal Function Recovery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004287
Enrollment
Unknown
Registered
2014-02-24
Start date
2014-03-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative ileus

Interventions

Chewing Gum (CG) Group:Chewing Gum

Sponsors

Tongji Hospital, Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Adult aged under 85 years; 2. Well-conscious; 3. Accept gastrointestinal surgery in our hospital; 4. Gender is unlimited; 5. BMI is unlimited; 6. Agree to participate in our RCT.

Exclusion criteria

Exclusion criteria: 1. Terrible-conscious; 2. Cannot chew; 3. Ileus before operation; 4. Ready to create stoma; 5. Refuse to participate in our RCT.

Design outcomes

Secondary

MeasureTime frame
Operation duration;Date of hospitalization;Cost of hospitalization;

Primary

MeasureTime frame
Time of flatus;Time of defecation;

Countries

China

Contacts

Public ContactHuang Qi

Department of Gastrointestinal Surgery of Tongji Hospital

hqhq007@hotmail.com+86 13524757117

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026