Clinical Trial

Outpatient Versus Inpatient Care Pathway for Intra-arterial Treatment of Primary Liver Cancer (CHOC)

Study acronym: CHOC
Recruiting
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Summary
Randomized multicentre trial comparing two care organisations (ambulatory vs conventional inpatient) for patients undergoing transarterial chemoembolization (TACE) or radioembolization (TARE) for primary liver cancer (Hepato Cellular Carcinoma (HCC) or intrahepatic cholangiocarcinoma (iCCA)). Patients are followed for 7 months to assess patient satisfaction, safety and clinical outcomes. A qualitative implementation study and a medico-economic evaluation (cost analysis and 5-years budget impact analysis) are embedded to assess acceptability, adoption, feasability, and sustainability and to inform scaling.
Protocol Amendment History 1 change
notable Trial sites expanded: 14 -> 19 locations 2026-07-01
Trial Details
NCT Number NCT06990659
Lead Sponsor University Hospital, Angers
Collaborators: Université Paris Cité
Conditions Hepato Cellular Carcinoma (HCC), Intrahepatic Cholangiocarcinoma
Enrollment 206 participants
Start Date 2025-12-18
Primary Completion 2027-12-17 (estimated)
Study Completion 2028-12-17 (estimated)
Updated on ClinicalTrials.gov 2026-07-17