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Clinical Study of XiangShaLiuJunZi Decotion Combined with S-1 as maintenance therapy for stage III or IV Gastric Carcinoma and Colorectal Carcinoma

Clinical Study of XiangShaLiuJunZi Decotion Combined with S-1 as maintenance therapy for stage III or IV Gastric Carcinoma and Colorectal Carcinoma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16008575
Enrollment
Unknown
Registered
2016-05-31
Start date
2016-06-01
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

advanced gastric cancer or colorectal cancer

Interventions

3:Observation group
2:S-1 plus Xiangsha Liujunzi Decoction group
1:S-1 group

Sponsors

Affiliated hospital of Guangdong Medicine College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Medical informed Consent must be signed by the patient or the witness; (2) The stage III/IV gastric cancer or colorectal cancer should be diagnosed by pathology or cytology; (3) The patients should be in control condition after chemotherapy (CR/PR/SD); (4) Aged from 18 to 75 years old; expected survival for more than 3 months; (5) The KPS score >=60; (6) According to RECIST 1.1, at least one target lesion is measurable; (7) Blood routine test: Hemoglobin>=90g/L; Neutrophil count>=1.5×10^9/LPlatelet count>=100×10^9/L; (8) Biochemical examination: STB=60ml/min.; (9) Heart and lung function is basically normal.

Exclusion criteria

Exclusion criteria: (1) The patients have heart, liver, kidney damage or abnormal bone marrow function at the same time; (2) The patients had other malignant tumors before or now, excepting the cutaneous basal cell carcinoma have been cured and the cervical carcinoma in situ; (3) The patients can not eat Chinese medicine because of poor body; (4) According to the investigator's judgment, there is a serious harm to the patient or the accompanying disease will obstruct patient to complete the study; (5) Pregnant or lactating women; (6) Being allergic to drugs used in the trial.

Design outcomes

Primary

MeasureTime frame
Treatment effect;

Countries

China

Contacts

Public ContactLiang Qilian

Affiliated hospital of Guangdong Medicine College

13822522910@163.com+86 0759-2387455

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 18, 2026