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Perioperative integrative medicine of fast track surgery and its application

Research on Traditional Chinese Medicine for fast recovery of postoperative gastrointestinal function

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-14005744
Enrollment
Unknown
Registered
2014-12-26
Start date
2014-12-01
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

laparoscopic surgery for colorectal cancer

Interventions

Interventinal Group:integrative medicine intervention
Control Group :Basic intervention

Sponsors

Guangdong Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients underwent laparoscopic surgery for colorectal cancer; 2. Aged from 45 to 75 years old; 3. The duration of operation is with 2 to 4 hours; 4. The anesthesia time is within 2.5 to 4.5 hours; 5. The TCM syndrome is identified as qi stagnation fu-organ stuff; 6. Willing to sign an informed consent document.

Exclusion criteria

Exclusion criteria: 1. Advanced malignant tumor cachexia, extremely weak; 2. Patients of malignant tumor who needs extended radical operation; 3. patients combined with cardiovascular, liver, kidney, brain, lung and other serious diseases, Bad drug control of Hypertension, diabetes; 4. Patients with mental disease; 5. Patients with allergies to the intervention; 6. Pregnant or breast-feeding women; 7. Severe malnutrition, serum albumin less than 21g/L, prealbumin less than 0.1g/L; 8. Re-abdominal surgery and severe intestinal adhesion; 9. Blood loss more than 400 milliliters during the surgery; 10. Occuring serious complications within 6 hours after the surgery, e.g. multiple organ dysfunction; 11. Postoperative intraperitoneal hyperthermic perfusion; 12. Emergency surgery; 13. Prokinetic drugs must be taken after operation; 14. Patient participating other clinical study or having participated other clinical study in the last one month; 15. Patient considered inappropriate to participate the study by clinical investigators.

Design outcomes

Primary

MeasureTime frame
time to first bowel sounds;time to first flatus;time to first defecation;Gastrointestal hormones;fatigue evaluation;recovery scale;

Countries

China

Contacts

Public ContactChen Zhiqiang
zhi57@163.com+86 020-81887233

Outcome results

None listed

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