OncoMatch

OncoMatch/Clinical Trials/NCT06394128

Cangpo Liujun Prescription on Cancer-related Fatigue in Advanced Colorectal Cancer With Spleen Deficiency and Dampness Excess

Is NCT06394128 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Cangpo Liujun Prescription for cancer-related fatigue.

Phase 2RecruitingFirst People's Hospital of HangzhouNCT06394128Data as of May 2026

Treatment: Cangpo Liujun PrescriptionThe goal of this clinical trial is to learn if Cangpo Liujun Prescription works to treat cancer-related fatigue in patients with advanced colorectal cancer undergoing second-line chemotherapy with spleen deficiency and dampness excess. It will also learn about the safety of Cangpo Liujun Prescription. The main questions it aims to answer are: Does Cangpo Liujun Prescription improve the fatigue symptoms for participants? How about the relationship between taking Cangpo Liujun Prescription and distribution of intestinal flora? Researchers will compare Cangpo Liujun Prescription to a placebo (a look-alike substance that contains no drug) to see if Cangpo Liujun decoction works to treat cancer-related fatigue in patients with advanced colorectal cancer undergoing second-line chemotherapy with spleen deficiency and dampness excess. Participants will: Take Cangpo Liujun Prescription or a placebo every day for 3 months Visit the clinic once every 2 weeks for checkups and tests Keep a diary of their symptoms Take blood samples to detect immune function and inflammatory factors Collected Feces for gut microbiota analysis

Check if I qualify

Extracted eligibility criteria

Cancer type

Colorectal Cancer

Disease stage

Required: Stage IV

Metastatic disease required

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Min 1 prior line

Lab requirements

Blood counts

No combined hematopoietic system diseases, such as anemia, requiring anemia correction drugs

Kidney function

serum creatinine < 1.5 times ULN

Liver function

ALT or AST < 5 times ULN; Bilirubin < 1.5 times ULN

Cardiac function

No heart failure or serious and difficult to control organic lesions

Patients with severe liver and kidney dysfunction (serum creatinine 1.5 times ULN; ALT or AST5 times ULN; Bilirubin 1.5 times ULN); Combined with hematopoietic system diseases, such as anemia, requiring anemia correction drugs; heart failure

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify