TACE
OtherControl arm will be treated by 2 or 3 cures of TACE DC beads at week 0, 8 and 16 (if required)
NCT Number: NCT01300143
Indication : Hepatocellular carcinoma, maximum size 9 cm, with single or multiple nodes whose total tumor mass can technically be irradiated, non-resectable, and not a candidate for percutaneous therapy with recommended treatment via hyperselective transarterial chemoembolisation (TACE).
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Notify Me18 year and older
All sexes
Interventional
Phase 2
CHU Amiens, Amiens, France
: Phase II controlled randomized trial, multicenter, comparing the benefit of additive conformational radiotherapy after therapy with hyperselective chemoembolisation (TACE) with treatment using three TACE treatments (standard of care).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Control arm will be treated by 2 or 3 cures of TACE DC beads at week 0, 8 and 16 (if required)
Experimental group will be treated by one cure of TACE DC Beads at week 0 then, within two weeks, by external conformational radiotherapy in 18 sessions
Time frame: up to 18 months
Time frame: within 90 days after the treatment
Time frame: after 90 days of treatment
Time frame: the day of randomization (week 0), at week 12 and week 24
Time frame: at week 24,week 48 and week 72
Time frame: up to18 months (week 72)
Time frame: within 3 years after first cure of TACE-DC BEADS
Nantes University Hospital
Other
Acronym: TACERTE
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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