Actively Recruiting
Observational Study of Intra Arterial Therapies for Primary Liver Cancer Evaluating Treatment Responses and Outcomes
Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2025-01-14
3300
Participants Needed
1
Research Sites
466 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying the best conditions for successful treatment outcomes in men and women with primary liver cancer using intra arterial therapy (IAT). This observational study focuses on hepatocellular carcinoma (HCC) and cholangiocarcinoma cancers, aiming to understand how these radiologic procedures that block blood supply to liver tumors affect patients. The study combines both retrospective and prospective data collection at the Radiology department of the IRCCS Azienda Ospedaliera Universitaria Hospital in Bologna. The study includes two phases: a retrospective phase analyzing radiological images from patients who received intra arterial therapy since January 1, 2009, with an expected enrollment of around 2000 participants, and a prospective phase enrolling about 1300 eligible participants over 5 years who will receive intra arterial therapy. Treatments studied include trans-arterial embolization (TAE), transarterial chemoembolization (TACE), transarterial radioembolization (TARE), and drug-eluting beads chemoembolization (DEB-TACE), all performed as part of routine clinical care. Participants will be monitored through clinical and radiological evaluations including CT scans and MRI to assess the type and size of the cancer, treatment response, and possible complications over a follow-up period extending up to 9 years. Researchers will collect data on injury type and size, radiological response, and post-treatment complications from enrollment through the end of treatment. The study aims to identify factors linked to optimal treatment responses and long-term outcomes.
CONDITIONS
Official Title
Intra Artherial Therapies in Treatment of Primary Liver Diseases: an Observational Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of hepatocellular carcinoma (HCC) or intrahepatic cholangiocarcinoma (iCCA) with clinical indication to receive or having received trans-arterial embolization (TAE), transarterial chemoembolization (TACE), transarterial radioembolization (TARE), or drug-eluting beads chemoembolization (DEB-TACE)
- Age over 18 years
- Ability to give informed consent
You will not qualify if you...
- Presence of shunt in gastrointestinal arteries that cannot be embolized
- Metastasis spread outside of the liver
- Liver failure
AI-Screening
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Trial Site Locations
Total: 1 location
1
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Bologna, Italy, 40138
Actively Recruiting
Research Team
C
Cristina Mosconi, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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