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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT02449967
Date of registration: 12/05/2015
Prospective Registration: No
Primary sponsor: Fuda Cancer Hospital, Guangzhou
Public title: HepaSphere Interventional Therapy Using Digital Subtraction Angiography(DSA) for Pancreatic Cancer
Scientific title: HepaSphere Interventional Therapy Using Digital Subtraction Angiography(DSA) for Pancreatic Cancer: Clinical Trial
Date of first enrolment: May 2015
Target sample size: 0
Recruitment status: Withdrawn
URL:  https://clinicaltrials.gov/show/NCT02449967
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).  
Phase:  Phase 1/Phase 2
Countries of recruitment
China
Contacts
Name:     Lizhi Liu, PhD
Address: 
Telephone:
Email:
Affiliation:  Fuda Cancer Hospital
Key inclusion & exclusion criteria

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: ?,?,?

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



Age minimum: 18 Years
Age maximum: 80 Years
Gender: All
Health Condition(s) or Problem(s) studied
Pancreatic Cancer
Intervention(s)
Procedure: interventional therapy
Primary Outcome(s)
Number of participants with Adverse events [Time Frame: 1 year]
Secondary Outcome(s)
Progress free disease (PFS) [Time Frame: 1 year]
Overall survival (OS) [Time Frame: 3 year]
Percentage of lesions that show no sign of recurrence 12 months after interventional therapy [Time Frame: 1 year]
Secondary ID(s)
Pancreatic Cancer HepaSphere
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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