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A Multicenter, Prospective Cohort Study on the Treatment of Early to Mid-Stage Colorectal Cancer Using Integrated Traditional Chinese and Western Medicine Based on the Integration of Disease and Syndrome.

A Multicenter, Prospective Cohort Study on the Treatment of Early to Mid-Stage Colorectal Cancer Using Integrated Traditional Chinese and Western Medicine Based on the Integration of Disease and Syndrome.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2025002469
Enrollment
Unknown
Registered
2025-12-24
Start date
2025-02-01
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Colorectal cancer

Interventions

Non-Exposed group:none
Exposure group:Chinese Herbal Compound Granules

Sponsors

Xiyuan Hospital, China Academy of Chinese Medical Science, Beijing, China.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) Colorectal cancer with definite pathological diagnosis and no evidence of distant metastasis, initially assessed as resectable colorectal cancer, clinical imaging stage I-III;(2) Patients who do not need neoadjuvant therapy after multidisciplinary discussion;(3) Age 18 to 85 years old, regardless of gender;(4) KPS score =70 points;(5) No history of colorectal cancer surgery or chemotherapy, no history of pelvic radiotherapy;(6) Patients read and sign the informed consent form of this study and agree to participate in this study.

Exclusion criteria

Exclusion criteria: (1) Patients who are receiving other types of anti-tumor or experimental therapy;(2) The patient is a pregnant or lactating woman;(3) Patients with severe cardiovascular and cerebrovascular disease complications, active hepatitis, and severe liver and kidney dysfunction;(4) Patients with complete intestinal obstruction who cannot be treated with oral drugs;(5) People who are allergic to the ingredients of the drug tested in this study;(6) The researcher decides that it is not suitable to participate in this researcher.

Design outcomes

Primary

MeasureTime frame
First postoperative exhaust time;

Secondary

MeasureTime frame
TCM syndrome and cold and heat scale score;Assessment of quality of life;Postoperative first bowel movement time;Postoperative complication incidence rate; Number of days in hospital after surgery;

Countries

China

Contacts

Public ContactYun Xu

Xiyuan Hospital, China Academy of Chinese Medical Science, Beijing, China.

839582256@qq.com15515847653

Outcome results

None listed

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