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A Multicenter Randomized control Study: Arsenic Trioxide plus Transcatheter Arterial Chemoembolization In Patients With Hepatocellular Carcinoma

The efficacy and safety of arsenic trioxide added transcatheter arterial chemoembolization in patients with hepatocellular carcinoma

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-09000523
Enrollment
Unknown
Registered
2009-08-27
Start date
2009-09-01
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

Hepatocellular carcinoma

Interventions

Group A:Epirubicin
Group B:Arsenic Trioxide
Group C:Epirubicin + Arsenic Trioxide

Sponsors

The first Hospital Affiliated to China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Male and Female patients aged 18 to 75 years old; 2. Histology or cytology confirmed in patients with primary liver cancer; or clinical diagnosis of liver cancer in line with standards (AFP increased a imaging, AFP is not high two kinds of imaging (CT + C, MR + C) check characteristic Performance; 3. At least one measurable lesion (bulky or nodular type); 4. BCLC stage: B to C phase; 5. ECOG score 0-2 points on the General Status; 6. Expected survival >=3 months; 7. liver function: Child A or B; 8. Able to follow-up with good compliance; 9. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Portal hypertension associated with portal vein tumor thrombus, collateral blood vessel formation was less; 2. Severe liver cell jaundice, liver failure or a large number of ascites; 3. Serious heart, kidney dysfunction, or coagulation dysfunction; 4. Liver tumor volume accounting for 70% or more; 5. Uncontrolled infection; 6. Pregnant or lactating patients; 7. Distant metastasis has occurred, lung metastasis; 8. Systemic failure; 9. Enrolled into the group lost to follow within the post-March.

Design outcomes

Primary

MeasureTime frame
Overall survival;Survival time;Quality of life scor;

Secondary

MeasureTime frame
Time to recurrence, TTR;Remission;Time to progression, TTP;

Countries

China

Contacts

Public ContactKe Xu
xuke@sina.vip.com+86 024 83282730

Outcome results

None listed

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