Evaluation of C-arm angiographic imaging system for abdominal intervention

Evaluation of C-arm angiographic imaging system for abdominal intervention - Evaluation of C-arm angiographic imaging system for abdominal intervention

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000019178

Enrollment

Registered

2015-10-01

Start date

2015-10-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

abdominal tumor

Interventions

Multi-phase C-arm CT imaging and PBV imaging will be taken one or more times (as necessary) during angiography

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who meet all the following criteria can be included in the study: 1. Patients have indication for abdominal angiography or intervention. 2. Written informed consent is obtained. 3. Adult (20 years old or older)

Exclusion criteria

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.

Design outcomes

Primary

Measure	Time frame
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	—

Countries

Japan

Contacts

Public ContactMasao Hamuro

Osaka City University Graduate School of Medicine Diagnostic and Interventional Radiology

hamuro@med.osaka-cu.ac.jp06-6645-3831

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026