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Prospective study of tansarterial embolization for hepatocellular carcinoma with Lipiodol added Lecithin.

Prospective study of tansarterial embolization for hepatocellular carcinoma with Lipiodol added Lecithin. - Tansarterial embolization for hepatocellular carcinoma with Lipiodol added Lecithin.

Status
Unknown
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000004312
Enrollment
60
Registered
2010-10-04
Start date
2007-04-01
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

hepatocellar carcinoma

Interventions

Lecithin Group:We use the emulsion which added the lecithin which is a surfactant in Lipiodol for transcatheter arterial embolization. Non-Lecithin Group:We use the Lipiodol which didn&#39
t add the lecithin for transcatheter arterial embolization

Sponsors

Tokyo Women's Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1:Histologically proven or clinically diagnosed hepatocellular carcinoma in primary lesion. 2:Age20-85 3:Performance Status0-1(ECOG) 4:Life expectancy at least 3 months. 5:Adequate organ and marrow function listed below. a.White blood cell(WBC):3,000<=WBC<12,000/uL b.Absolute neutrophil count(Neu):Neu >=1,800/uL c.Hemoglobin(Hb): Hb>=8.0g/dL d.Serum creatinine(Cr):W.N.L e. Electrocardiogram(ECG):normal 6:Do not become the adaptation of resection,transplant,and local treatment in algorithm of HCC treatment. 7:Without contraindication of TAE. 8:The patient who have given written informed consent to participant in this study.

Exclusion criteria

Exclusion criteria: 1:The patient with the anamnesis of the drug hypersensitivity. 2:The patient with contraindication of medication(Hydrochloric acid doxorubicin, Lipiodol, Gelpert and lecithin). 3:The patient with contraindication of TAE. a.Severe liver failure b.Serum Bilirubin(T-Bil):T-Bil>3mg/dl c.Large quantities of acites. 4:The patient having the activity-related infectious disease(more than fever 38.0 degrees ).

Design outcomes

Primary

MeasureTime frame
curative effect,response rate,survival time, survival rate

Secondary

MeasureTime frame
adverse events

Countries

Japan

Contacts

Public ContactYutaka Takahashi

Tokyo Women's Medical University Department of Surgery, Institute of Gastroenterology

yutaka@ige.twmu.ac.jp

Outcome results

None listed

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