Evaluation of C-arm angiographic imaging system for abdominal interventio
Not Applicable
- Conditions
- abdominal tumor
- Registration Number
- JPRN-UMIN000019178
- Lead Sponsor
- Osaka City University Graduate School of Medicine Diagnostic and Interventional Radiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who meet any of the following criteria are not eligible for the study: 1. Patients have contraindication to contrast media. 2. Patients are currently or intending to become pregnant or are lactating. 3. Inadequate physical condition judged by the physician.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome: tumor number, tumor morphology, tumor contrast effect, vascular occlusion range, hepatic blood flow, hepatic volume Evaluation period: dynamic contrast enhanced CT within 3months before and after intervention, multi-phase C-arm CT imaging and PBV imaging during intervention
- Secondary Outcome Measures
Name Time Method