cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. healthy volunteer group Inclusion criteria: Healthy body; Age 18-80 years old; No diabetes, heart, cerebrovascular system, immune system and other diseases, Blood, urine routine, liver, kidney function is normal; No virus, bacterial infection and other diseases; Volunteer and have signed the consent of the consent. 2. group of malignant tumor patients Inclusion criteria: Consistent with the diagnostic criteria for malignant tumors; (ICD-10) diagnostic criteria for cancer-related fatigue, that is, fatigue symptoms recur, the duration of more than 2 weeks, accompanied by the following symptoms in five or more: Physical activity is difficult to recover; there are emotional reactions, such as sadness, frustration or irritability; can not complete the original can not be completed; Competent daily activities; short-term memory loss; fatigue symptoms can not be alleviated for hours; Age 18-70 years old; Expected survival> 6 months; Physical condition (EOCG) score below 2 points; Primary school or higher, no cognitive impairment; Good compliance, willing to cooperate with the study, to accept the relevant treatment and the physical and chemical examination; Informed consent and signed informed consent.
Exclusion criteria
Exclusion criteria: Health volunteer exclusion criteria: Those who do not meet the criteria; (SDS) standard points 109-115 higher than 53 points, or anxiety self-rating scale score (SAS) standard points 194-197 higher than 50 points. There is history of drug and alcohol dependence. Unaware and unable to cooperate with; Allergic constitution (allergic to Class 2 or above), or allergic to the ingredients of this preparation; Pregnancy, lactation and preparation of pregnant women; Those who participated or participated in other clinical trials within one month. Malignant Tumor Patients Exclusion criteria: Those who do not meet the criteria; Combined with important organ dysfunction and the immune system of primary disease; Recent serious infection; (SDS) standard points 109-115 higher than 53 points, or anxiety self - rating scale score (SAS) standard points 194-197 higher than 50 points; Unaware and unable to cooperate with; Combined with heart, brain, lung, liver and kidney system serious primary disease; Allergic constitution (allergic to Class 2 or above), or allergic to the ingredients of this preparation; Pregnancy, lactation and preparation of pregnant women; Those who participated or participated in other clinical trials within one month.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Simple Fatigue Scale;Cancer treatment function evaluation fatigue scale;Multidimensional fatigue symptoms scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Clinical remission rate;TCM Syndrome grading quantitative assessment;Tumor marker; | — |
Countries
China
Contacts
First Teaching Hospital of Tianjin University of Traditional Chinese Medicine