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

F

Fuda Cancer Hospital, Guangzhou

Status and phase

Withdrawn
Phase 2
Phase 1

Conditions

Pancreatic Cancer

Treatments

Procedure: interventional therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT02449967
Pancreatic Cancer HepaSphere

Details and patient eligibility

About

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

Full description

By enrolling patients with pancreatic 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 pancreatic cancer.

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  • Patients with other primary tumor except pancreatic cancer
  • History of coagulation disorders or anemia

Trial design

0 participants in 2 patient groups

HepaSphere
Experimental group
Description:
pancreatic cancer patients received HepaSphere interventional therapy using the digital subtraction angiography(DSA)
Treatment:
Procedure: interventional therapy
control
No Intervention group
Description:
pancreatic cancer patients did not receive any interventional therapy

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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