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Clinical Study on the Yikousizi San Topical Application to Promote Gastrointestinal Function Recovery Following Colon Cancer Surgery

Clinical Study on the Yikousizi San Topical Application to Promote Gastrointestinal Function Recovery Following Colon Cancer Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001067
Enrollment
Unknown
Registered
2026-04-24
Start date
2026-04-30
Completion date
Unknown
Last updated
2026-04-28

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

Conditions

Colorectal cancer

Interventions

Control group:ERAS Basic Management
Experimental group:ERAS Combined with Yikousizi San hot compress

Sponsors

Guangdong Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1: Patients who meet the Western medical diagnostic criteria outlined in the Chinese protocol of diagnosis and treatment of colorectal cancer(2020 edition), have undergone laparoscopic curative surgery, and were preoperatively staged as high-risk Stage II or Stage III on CT 2: Aged 18–75, regardless of gender 3: KPS > 60 points, with an expected survival period of >6 months 4: Have not recently taken antibiotics, hormones, probiotics, gastrointestinal motility agents, traditional Chinese medicine, or other medications that affect the intestinal microbiota 5: Demonstrate good compliance and are able to tolerate drug therapy 6: Are able to cooperate with this study and provide timely feedback on medication use and treatment status 7: Voluntarily participate in this study and sign an informed consent form

Exclusion criteria

Exclusion criteria: 1: Patients with severe underlying diseases of the cardiovascular, cerebrovascular, hepatic, renal, or hematopoietic systems 2: Patients with a history of or concurrent malignant tumors 3: Patients with drug allergies 4: Patients with cognitive or psychiatric disorders 5: Patients who intend to become pregnant in the near future, are currently pregnant, or are breastfeeding 6: Patients currently participating in other clinical drug trials

Design outcomes

Primary

MeasureTime frame
Recovery time for bowel sounds;Time of first postoperative exhaust and defecation;

Secondary

MeasureTime frame
Gastrointestinal Symptom Rating Scale;Fatigue Scale;Oxygen Radical Detection;Rehabilitation Scale;Inflammatory factors;Gastrointestinal hormones;

Countries

China

Contacts

Public ContactDiao Jingfang

Guangdong Hospital of Traditional Chinese Medicine

diaojingfang@126.com13751780314

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: May 1, 2026