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Ameliorative Effect of Transcutaneous Electrical Acustimulation on pain induced by TACE in patients with Hepatocellular Carcinoma: a Multi-Center Randomized Controlled Study

Ameliorative Effect of Transcutaneous Electrical Acustimulation on pain induced by TACE in patients with Hepatocellular Carcinoma: a Multi-Center Randomized Controlled Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300067941
Enrollment
Unknown
Registered
2023-02-01
Start date
2023-02-01
Completion date
Unknown
Last updated
2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatocellular Carcinoma

Interventions

Group A:transcutaneous electroacupuncture, TEA
Group B:sham transcutaneous electroacupuncture

Sponsors

Shanghai Changzheng Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Willing to sign the informed consent; 2. Aged 18-75, both sexes; 3. Clinical diagnosis of primary hepatocellular carcinoma; 4. Child-Pugh A/B liver function, ECOG PS score 0-1; 5. Barcelona lesions (BCLC) stage A, B and some C, suitable for TACE.

Exclusion criteria

Exclusion criteria: 1. History of other malignant tumors within 5 years 2. Taking analgesics, antidepressants, anti-epileptic drugs and other drugs within 6 months; 3. serious cardiovascular and cerebrovascular diseases; 4. diabetic blood glucose that cannot be controlled; 5. Cognitive dysfunction, aphasia, mental disorders or diseases that may affect patients' cooperation; 6. pregnant, preparingn for pregnancy or breastfeeding patients; 7. Severe liver dysfunction: Child-Pugh grade C liver function, serum bilirubin > 51.3 µmol/L, hepatic encephalopathy, refractory abdominal effusion or hepatorenal syndrome, etc. 8. Irreversible severe coagulopathy: INR > 1.5, platelet < 50 x10^9; 9. Complete tumor thrombus or thromboembolism of the main portal vein, with poor formation of collateral vessels; 10. Severe infection or complicated with active hepatitis that cannot be treated simultaneously; 11. Familiar with acupuncture treatment, acupoint selection or meridians; 12. Skin diseases affecting electrode fixation; 13. In the opinion of the researcher, it is not suitable for participants.

Design outcomes

Secondary

MeasureTime frame
VAS;Dose of morphine;Nausea and vomiting score;HRV;EGG;IL-6;NE;TNF-a;IL-1ß;NGF;

Primary

MeasureTime frame
VAS;the ratio of morphine use;

Countries

China

Contacts

Public ContactWeihua Dong

Shanghai Changzheng Hospital

dongweihua@smmu.edu.cn+86 13801706946

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026