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Study on the clinical efficacy of JPBSF with the chemotherapy treatment of patients after colorectal surgery

mechanism research on recurrence or metastasis of JPBSF with the treatment of patients after colorec

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004899
Enrollment
Unknown
Registered
2014-05-29
Start date
2013-05-01
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

after curative resection of colorectal cancer

Interventions

Trial group:Traditional Chinese medicine
Control:Traditional Chinese medicine

Sponsors

Putuo Hospital, Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. volunteered to participate in this study and signed an informed consent form; 2.there is a clear pathological diagnosis of colorectal cancer patients after radical surgery; 3.TMN staging Phase II or III; 4.do standard adjuvant chemotherapy, expected survival more than 3 months; 5. TCM reference to Chinese medicine clinical research guidelines (third series) developed by the People's Republic of China Ministry of Health; 6. no serious disorders in heart, liver, kidney, and hematopoietic system, chemotherapy contraindications, and other drug evaluation factors; 7 .Age from 18 to 75 years old, no sex limit; 8 .Karnofsky score more than 70 points.

Exclusion criteria

Exclusion criteria: 1.do not meet the inclusion criteria above; 2.the patients with abdominal or hepatic recurrence or metastasis; 3.significant heart (history of severe heart disease, such as coronary heart disease,myocardial infarction and so on), liver (ALT, AST has obvious abnormalities), kidney (CKD stage> 2) or other function damage, mentally ill, pregnant or lactating women; 4. allergies or multiple drug allergies; 5. patients participated in other clinical trials, before the trial three months ago.

Design outcomes

Primary

MeasureTime frame
VEGF;Immune functionCD3, CD4;Tumor markers CA199, CE;

Secondary

MeasureTime frame
Piper Fatigue Scale;TCM Syndrome Rating Scal;

Countries

China

Contacts

Public ContactYIN PEIHAO
yinpeihao1975@hotmail.com+86 13636305607

Outcome results

None listed

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