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Clinical research on external application of Shuangbai San for cancer pain due to primary liver cancer

Clinical research on external application of Shuangbai San for cancer pain due to primary liver cancer

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-11001384
Enrollment
Unknown
Registered
2011-06-10
Start date
2010-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

primary liver cancer.

Interventions

Mild pain group:External application of Shuangbai San or placebo (Treating burst pain with tramadol injection)
Moderate-severe pain group:External application of Shuangbai San or placebo + orally taking morphine sulfate (treating burst pain with morphine injection)

Sponsors

Guangzhou University of TCM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Clinical and pathological confirmed primary liver cancer Diagnosis standard is according to the cancer fascicule of clinical diagnosing and treating guideline (2005); 2. Patients with pain in upper abdomen or liver area; 3. Predicted survival>2 months; 4. Karnosfskye score>=20; 5. Aged 18-85 yrs; 6. No history of drug abuse or allergy; 7. Voluntarily signed the informed consent and having good adherence.

Exclusion criteria

Exclusion criteria: 1. Patients with severe heart, brain, kidney, hematology or psychological disease; 2. Severe pain due to the primary liver cancer combined with liver rupture and bleeding; 3. Severe complications such as refractory ascites, biliary fistula, Intraperitoneal infection, GI bleeding, hepatic failure and intraperitoneal bleeding, etc.; 4. Pregnant or lactating women; 5. Allergic to multiple medicine or trial drug; 6. Experienced operation, interventional therapy, radiofrequency ablation or neural blocking therapy 1 week before the trial; 7. Patients who are considered not suitable for the trial by the researcher.

Design outcomes

Primary

MeasureTime frame
Quality of life, simple pain questionnair, digital pain evaluation;

Secondary

MeasureTime frame
ß-endorphin;

Countries

China

Contacts

Public ContactXiaowei Ye
billye983@yahoo.com.cn+86 13503016923

Outcome results

None listed

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