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Prediction of residual liver hypertrophy by liver iodine map

Study on liver iodine map by portal vein angiography and prediction of expected residual hepatic hypertrophy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1041210088
Enrollment
199
Registered
2021-10-22
Start date
2021-11-11
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

Primary or metastatic liver cancer or biliary tract cancer Liver cancer, biliary tract cancer

Interventions

Two dual enrgy CT scans, simple CT and contrast CT, during portal vein embolization
D003287, D015898
iodine contrast media, X-ray exposure

Sponsors

Komada Tomohiro
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with primary or metastatic liver cancer or biliary tract cancer who are scheduled for extended hepatectomy and will undergo portal vein embolization Written consent must be obtained.

Exclusion criteria

Exclusion criteria: contraindicated patients for iodine contrast administration Decreased renal function (eGFR less than 30 mL/min/1.73m2)

Design outcomes

Primary

MeasureTime frame
Liver volumes of embolized and unembolized lobes and their rates of change before and after portal vein embolization

Secondary

MeasureTime frame
Complications due to portal vein embolization (e.g., liver dysfunction and portal vein thrombus), presence of liver failure after extended hepatectomy, length of hospital stay, and survival

Contacts

Public ContactTomohiro Komada

Nagoya university hospital

tidai@med.nagoya-u.ac.jp+81-52-744-2327

Outcome results

None listed

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