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An exploratory study on the treatment of stage III colon cancer with special prescription of removing dampness and removing dampness after postoperative chemotherapy

An exploratory study on the treatment of stage III colon cancer with special prescription of removing dampness and removing dampness after postoperative chemotherapy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034064
Enrollment
Unknown
Registered
2020-06-22
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-06-29

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

Conditions

Colon cancer

Interventions

Sponsors

Oncology Department, Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with colon cancer confirmed by histopathology or cytopathology; 2. Patients who have undergone radical surgery and whose postoperative pathological stage is stage III and T4 or N2 (according to NCCN clinical practice guideline colorectal cancer (2018 V4) standard); 3. Adjuvant chemotherapy has been completed (for example, 4-8 XELOX, 6-12 FOLFOX, or fluorouracil single drug chemotherapy has been completed, and no adjuvant chemotherapy will be accepted in the near future); 4. The patients without recurrence and metastasis were reexamined in the past 1 month; 5. Patients whose last chemotherapy time was less than 3 months; 6. Patients with PS score (ECoG) = 60ml / min; Normal liver function: total serum bilirubin level <= 1.5 times of upper limit of normal value (ULN), serum AST and ALT 2.5 times of ULN; 9. The patients who sign the informed consent and are willing to receive the treatment of this program, can insist on taking medicine and have good compliance.

Exclusion criteria

Exclusion criteria: 1. Patients who are unable to complete the baseline assessment form; 2. Patients with ileus or incomplete ileus; 3. Patients with other serious diseases, including uncontrolled active infection, severe electrolyte disorder, and obvious bleeding tendency; 4. Pregnant and lactating women; 5. Patients with autoimmune diseases and blood system diseases, or long-term use of hormone or immunosuppressant; 6. Patients with other uncontrolled tumors; 7. Patients who have received new adjuvant or adjuvant radiotherapy, or intend to receive radiotherapy; 8. Patients with serious brain disease or mental disease that affect the ability of self-report; 9. Have a history of organ transplantation (including bone marrow autotransplantation and peripheral stem cell transplantation); 10. Patients without legal capacity, and those who are affected by medical or ethical reasons.

Design outcomes

Primary

MeasureTime frame
3 year recurrence and metastasis rate;

Secondary

MeasureTime frame
1 year recurrence and metastasis rate;2 year recurrence and metastasis rate;

Countries

China

Contacts

Public ContactHaibo Zhang

Guangdong Provincial Hospital of Traditional Chinese Medicine

haibozh@gzucm.edu.cn+86 13724123615

Outcome results

None listed

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