Breast Cancer
Conditions
Interventions
Experimental group:Probiotic solid drink
Control group:Placebo solid drink
Sponsors
Tangshan Central Hospital
Eligibility
Sex/Gender
Female
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Newly diagnosed breast cancer patients who are planning to undergo chemotherapy; 2. Aged 20 to 60 years; 3. No immune system disease; 4. Agree to participate in this study and sign the informed consent.
Exclusion criteria
Exclusion criteria: 1. Suffering from refractory oral ulcers, psoriasis, eczema, tinea pedis and other skin diseases, and other diseases that may cause skin damage (such as syphilis, etc.); 2. Suffering from severe gastrointestinal diseases (such as gastrointestinal ulcers, gastrointestinal perforation, ulcerative colitis, irritable bowel syndrome, etc.); 3. Those with coronary heart disease, myocardial infarction and extremely poor heart function; 4. Participating in other clinical trials; 5. Patients with severe liver and kidney disease; 6. Suffering from dementia (defined as MMSE score <= 2 points) or Parkinson's disease or other neurological diseases that cause dysfunction, as well as a history of traumatic brain injury, cerebral hemorrhage, stroke, brain tumor, cerebral infarction, etc.; 7. Advanced patients or patients with other malignant tumors; 8. Those who have mental illness or have a family history of mental illness; 9. Patients who are addicted to alcohol or drugs; 10. Those who refuse to join the group and cannot cooperate with the treatment; 11. The attending doctor or the researcher believes that there are other circumstances that are not suitable for participating in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| side effects; | — |
Secondary
| Measure | Time frame |
|---|---|
| Gut microbiota; | — |
Countries
China
Contacts
Public ContactZhang Juan
Tangshan Central Hospital
Outcome results
None listed