endocrine therapy-related hot flashes
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Age older than (including) 18 years, less than (including) 75 years; 2. Hormone receptor positive breast cancer patients; 3. Use EP at least 30 days before the study, and plan to continue treatment during the study period; 4. After EP use, the following symptoms begin to appear or aggravate: hot flashes, can be accompanied by night sweating, insomnia, fatigue, depression, loss of libido, quality of life. Amount decreased; 5. Patients with hot flashes: frequency of hot flashes (> 3 times per day); 6. KPS > 70 points, ECOG physical state 0-2 points.
Exclusion criteria
Exclusion criteria: 1. Pregnant or lactating women, or those who have fertility requirements in the past six months; 2. Acupuncture and moxibustion treatment for adverse endocrine symptoms in the first three months of the study; 3. Drug therapy for menopausal symptoms (such as systemic phytoestrogen, tebron or similar substances, venlaxine or specific homeopathic drugs) is currently being used; 4. Research process Patients planning to undergo surgery, chemotherapy, radiotherapy and immunotherapy; 5. History of other malignant tumors in the past five years; 6. Severe coagulation dysfunction; 7. History of cardiovascular, liver, respiratory, kidney, blood and endocrine diseases with clinical symptoms; 8. Mental or cognitive impairment; 9. Researchers do not consider it appropriate to participate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| hot flash score; | — |
Secondary
| Measure | Time frame |
|---|---|
| timing of hot flash;Severity of sweating;Kupperman;Functional Assessment of Cancer Therapy-Breast cancer; | — |
Countries
China
Contacts
The First Affiliated Hospital of Nanjing Medical University, Jiangsu Privnce Hospital