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Phase II trial of embolization with NBCA-lipiodol mixture (JIVROSG-0802)

Phase II trial of embolization with NBCA-lipiodol mixture (JIVROSG-0802) - Phase II trial of NBCA (JIVROSG-0802)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000012564
Enrollment
65
Registered
2013-12-12
Start date
2014-02-01
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

active bleeding, pseudoaneurysm, true aneurysm, vascular malformation, arteriovenous fistula, and embolization in vascular intervention

Interventions

arterial embolization with NBCA-lipiodol

Sponsors

Japan Interventional Radiology In Oncology Study Group(JIVROSG)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who will undergo arterial embolizaiton for the pathophysiologies listed below. Active bleeding or pseudoaneurysm True aneurysm Vascuar malformation Arteriovenous fistula Arterial re-distribution 2. Difficulties in embolization with pre-existing embolic materials approved in Japan judged by radiologists. or Failures of embolization with pre-existing embolic materials approved in Japan. 3. Shock index < 1.5 4.Written informe consent is obtained from patients or their relatives.

Exclusion criteria

Exclusion criteria: 1. Allergic histories for iodininated contrast medium or lipiodol. 2. CNS arteriovenous malformation 3. Cerebral aneurysm 4. DIC 5. Uncontrollable shock 6. Endoleak after aortic stent placement 7. Pregnant woman, or pegnancy is suspected 8. Radiologist judged that the patients is not suitable for the present study.

Design outcomes

Primary

MeasureTime frame
Efficacy: Success rate of embolization with NBCA-lipiodol mixture

Secondary

MeasureTime frame
Safety: Frequency of adverse events

Countries

Japan

Contacts

Public ContactShunsuke Sugawara

National Cancer Center Diagnostic Radiology

sugasuga_shun@yahoo.co.jp03-5475-5201

Outcome results

None listed

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