Cancer Pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Pathologically confirmed malignant tumor, accompanied by pain caused by tumor progression/invasion or by antitumor therapy; (2) Aged 18 to 80 years, with an expected survival of = 3 months; (3) Moderate to severe pain, defined as a Visual Analogue Scale (VAS) score = 4; (4) Conscious, with sufficient comprehension and communication skills required for the study, and voluntarily providing signed informed consent.
Exclusion criteria
Exclusion criteria: 1) Pain associated with oncological emergencies, such as fracture, visceral organ obstruction, or perforation; 2) Severe organ dysfunction such as end-stage renal disease, severe heart failure, and difficult-to-control infections; 3) Pregnant or breastfeeding women; 4) Patients with consciousness disorders, mental disorders, or communication disorders who are unable to complete study questionnaires or scale assessments; 5) Local infection or inflammation at the acupuncture site with tumor infiltration; 6) Coagulation dysfunction (INR > 1.5), platelet count < 100 × 10^9/L; 7) Use of non-opioid analgesics (e.g., NSAIDs, anticonvulsants, antidepressants), implantable analgesic pumps, nerve blocks, or other invasive pain treatments within the past 1 month; 8) Patients with non-removable electronic devices or metal implants that may interfere with bioelectrical signal collection; 9) Exclusion of long-term use of immunosuppressants or high-dose corticosteroids
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Difference in Visual Analogue Scale scores before and after treatment; | — |
Secondary
| Measure | Time frame |
|---|---|
| visual analogue scale;Brief Pain Inventory;Karnofsky Performance Status scale;Change in opioid consumption; | — |
Countries
China
Contacts
Guangzhou University of Chinese Medicine Shenzhen Hospital(Futian)