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HepaSphere Interventional Therapy Using Digital Subtraction Angiography(DSA) for Liver Cancer

HepaSphere Interventional Therapy Using Digital Subtraction Angiography(DSA) for Liver Cancer: Clinical Trial

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02447263
Enrollment
87
Registered
2015-05-18
Start date
2015-05-31
Completion date
2016-02-29
Last updated
2016-02-25

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

Conditions

Liver Cancer

Keywords

Liver Cancer, HepaSphere

Brief summary

The purpose of this study is to evaluate the safety and efficacy of HepaSphere interventional therapy using digital subtraction angiography(DSA) for liver cancer.

Detailed description

By enrolling patients with liver cancer adapted to enrolled criteria, this study will document for the first time the safety and the short and long term efficacy of HepaSphere interventional therapy using digital subtraction angiography(DSA) for liver cancer.

Interventions

liver cancer patients received HepaSphere interventional therapy using the digital subtraction angiography(DSA)

Sponsors

Fuda Cancer Hospital, Guangzhou
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Age:18-80 2. Karnofsky performance status \>60 3. Diagnosis of pancreatic cancer based on histology or the current accepted radiological measures. 4. Classification tumor,nodes,metastasis-classification(TNM) stage: Ⅱ,Ⅲ,Ⅳ 5. Will receive interventional therapy 6. Life expectancy: Greater than 3 months 7. Patients' routine blood test, liver function and kidney function have no obvious abnormalities 8. Ability to understand the study protocol and a willingness to sign a written informed consent document

Exclusion criteria

1. Patients with other primary tumor except pancreatic cancer 2. History of coagulation disorders or anemia

Design outcomes

Primary

MeasureTime frame
Number of participants with Adverse events1 year

Secondary

MeasureTime frame
Percentage of lesions interventional therapy that show no sign of recurrence 12 months after1 year
Progress free disease (PFS)1 year
Overall survival (OS)3 year

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026