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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03716063
Other study ID # httxixi
Secondary ID
Status Not yet recruiting
Phase Phase 3
First received
Last updated
Start date October 30, 2018
Est. completion date December 30, 2021

Study information

Verified date October 2018
Source Xiyuan Hospital of China Academy of Chinese Medical Sciences
Contact yu wu, master
Phone 010-62835438
Email 18813084816@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will take disease-free survival time and recurrence and metastasis rate as the main evaluation indexes, to evaluate the clinical efficacy of strengthening the spleen and reducing phlegm method in patients with stage II high-risk and stage III colorectal cancer


Description:

The study enrolled 350 patients with stage II high-risk and stage III colorectal cancer who underwent adjuvant chemotherapy (based on a 5-fluorouracil(5-FU) regimen for at least 3 months) and patients who received chemotherapy for less than 3 months. The study will use a large sample, multicenter, randomized, double-blind study. The experimental group was given oral Jianpi Huatan dispensing granule, once a day in the morning and evening, 1 course per 1 month, a total of 3 courses; the control group of oral Chinese medicine formula low dose control granules (including the test group dose 1 /10), 1 time each morning and evening, 1 course per month, for a total of 3 courses.

The patients were followed up once a month during the treatment period and once every 3-6 months after the end of treatment until the patient relapsed, died or the study was over.Some patients in the study will be tested for circulating tumor cells.

Main outcome measures is Disease-free survival time(DFS)and Metastasis recurrence rate in 1 year;Secondary outcome measures:Quality of life score: applied quality of life scale.Metastasis recurrence rate in 2、3years.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 350
Est. completion date December 30, 2021
Est. primary completion date December 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

1. Patients with colorectal cancer with clear pathological diagnosis and Western medicine diagnostic criteria;

2. Radical resection of colorectal cancer was performed and adjuvant chemotherapy (based on 5-FU regimens for at least 3 months) was completed within 3 months of the end of chemotherapy;

3. Tumor Node Metastasis(TNM) stage is high-risk II stage and III stage;

4. Age 18-80 years, sex unlimited;

5. No recurrence or metastasis by imaging or doctor's clinical judgement;

6. Signed informed consent; Note * According to National Comprehensive Cancer Network(NCCN )clinical guidelines: Phase II:T3-4N0M0; High-risk Phase II is defined as follows::a.T4;b. Less than 12 lymph nodes were detected;c. preoperative intestinal obstruction, perforation of tumor site;d. poor histological differentiation (except highly unstable microsatellite);e. neurological invasion and vascular tumor thrombus; f. positive or unknown margin, and insufficient margin safety distance. Phase III:T1-4N1-2M0.

Exclusion criteria:

1. History of previous or combined malignancies except cured basal cell carcinoma of the skin and carcinoma in situ of the cervix;

2. Combined with severe heart, liver and kidney disease;

3. Any unstable condition or condition that may endanger patient safety and compliance with research, such as pregnancy, depression, manic-depressive disorder, obsessive-compulsive disorder, or schizophrenia;

4. The researchers determine that they were not suitable for the study.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Jianpi Huatan dispensing granule
once a day in the morning and evening, every month for a course of treatment, a total of three courses

Locations

Country Name City State
China Xiyuan Hospital, China Academy of Chinese Medical Sciences Peking Beijing

Sponsors (3)

Lead Sponsor Collaborator
Xiyuan Hospital of China Academy of Chinese Medical Sciences Chinese Academy of Medical Sciences, Tianjin People's Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Disease-free survival time from the date of radical resection of colorectal cancer to the time of recurrence or metastasis. 3 years
Primary Metastasis recurrence rate in 1 year The ratio of metastasis and recurrence to the patients was observed. 1 year
Secondary Traditional Chinese Medicine(TCM )symptom grading table Effective: after treatment, TCM symptom score decreased by more than 50% compared with that before treatment.
Effective: decrease < 50% and equal to 30%; Invalid: decrease < 30%. Note: the formula is: (before treatment - integral after treatment) / before treatment by 100%
3 months
Secondary Functional Assessment of Cancer Therapy-Colorectal (FACT-C) scale The FACT-C scale was divided into five grades: none (0), one point (1), some (2), equivalent (3) and very (4). The positive items (i.e. the higher the grade, the better the quality of life.) 3 months
Secondary Edmonton Symptom Assessment Scale( ESAS ) The scale used digital scoring method, each symptom scoring range of 0-10 points, 0 points for asymptomatic, 10 points for the most serious degree imaginable, patients choose a number to express their subjective feelings, the larger the number indicates the more serious the symptoms. 1~10 points were divided into 3 degrees, mild, moderate and severe. 1~3 were mild, 4~6 were moderate, and 7~10 were severe 3months
Secondary Metastasis recurrence rate in 2 years The ratio of metastasis and recurrence to the patients was observed. 2 years
Secondary Metastasis recurrence rate in 3 years The ratio of metastasis and recurrence to the patients was observed. 3 years
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