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Study on the pain of cancer caused by the combination of electric needle ear acupuncture and drugs on renal deficiency blood stasis bone metastasis

Phase 1
Completed
Conditions
Bone metastatic cancer pain
Registration Number
ITMCTR2100005442
Lead Sponsor
Huangpu Street Community Health Service Center, Huangpu District, Guangzhou
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Histological or cytologically confirmed malignancy and clinical manifestations by X-ray, CT, MRI, ECT, or PET-CT tests combined with bone metastatic carcinoma. The syndrome is consistent with patients with renal deficiency and blood stasis. (1) Age 30 to 75 years old, estimated survival period greater than 1 month; (2) According to the 2015 U.S. Clinical Practice Guidelines for Cancer Pain in Adults, the cause of cancer pain is directly caused by tumors, including pain caused by primary tumors and/or metastatic tumors; pain caused by tumor treatment; pain associated with tumors; (3) bone pain associated with bone metastases of tumors and cancer pain NRS (Pain Numerical Assessment Method) > 4 points; (4) Kamofsky Performance Status (KPS) = 60 points; (5) Normal language expression ability, judgment ability of their general condition and pain, good compliance, and can express and evaluate pain with cooperative researchers.

Exclusion Criteria

(1) Severe pain before treatment, NRS = 9 points, morphine dosage is large but still can not relieve pain; (2) within one month of the tumor site or pain site used radiotherapy, chemotherapy or nerve blockade therapy; (3) non-cancer pain, such as surgical incision pain, etc.; (4) combined severe heart, liver, kidney, hematopoietic system insufficiency, etc.; (5) halo needles or fear or resistance to acupuncture treatment; (6) intellectual disabilities or accompanied by hearing, mental, cognitive, and cognitive impairment; (7) participants in other research projects.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
RS;
Secondary Outcome Measures
NameTimeMethod
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