A randomised parallel group study to compare transarterial particle embolism with percutaneous ethanol injection in patients with unifocal, small (<3cm), non-resectable hepatocellular carcinoma

ISRCTN ISRCTN54481540
DOI https://doi.org/10.1186/ISRCTN54481540
Protocol serial number N0256159469
Sponsor Department of Health
Funders The Royal Free Hampstead NHS Trust (UK), NHS R&D Support Funding
Submission date
30/09/2005
Registration date
30/09/2005
Last edited
26/10/2015
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Cancer
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Not provided at time of registration

Contact information

Prof Andrew K Burroughs
Scientific

Department of Liver Medicine & Transplantation
Royal Free Hampstead NHS Trust
Pond Street
Hampstead
London
NW3 2QG
United Kingdom

Study information

Primary study designInterventional
Study designRandomised parallel-group study
Secondary study designRandomised controlled trial
Study type Participant information sheet
Scientific titleA randomised parallel group study to compare transarterial particle embolism with percutaneous ethanol injection in patients with unifocal, small (<3cm), non-resectable hepatocellular carcinoma
Study objectivesWhich is the best treatment in terms of survival of patients diagnosed with unresectable unifocal hepatocellular carcinoma (HCC) less than 3 cm in diameter treated with percutaneous ethanol injection or transarterial particle embolisation?
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedCancer: Liver
InterventionPercutaneous ethanol injection or transarterial particle embolisation
Intervention typeDrug
PhaseNot Applicable
Drug / device / biological / vaccine name(s)Ethanol
Primary outcome measure(s)

Survival of patient after treatment of unresectable, unifocal, small (3 cm) hepatocellular carcinoma

Key secondary outcome measure(s)

Not provided at time of registration

Completion date31/07/2006

Eligibility

Participant type(s)Patient
Age groupNot Specified
SexNot Specified
Target sample size at registration185
Key inclusion criteriaNot provided at time of registration
Key exclusion criteriaNot provided at time of registration
Date of first enrolment31/07/2003
Date of final enrolment31/07/2006

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

Royal Free Hampstead NHS Trust
London
NW3 2QG
United Kingdom

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Participant information sheet Participant information sheet 11/11/2025 11/11/2025 No Yes