Observing the effects of intra-arterial therapies for liver cancer
Official title: Intra Artherial Therapies in Treatment of Primary Liver Diseases: an Observational Study
Run by IRCCS Azienda Ospedaliero-Universitaria di Bologna · NCT06774690 · Data updated 2026-11-12
This study is trying to find the best ways to help people with liver cancer get better results from a treatment called intra-arterial therapy.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 3300 (estimated) |
| Sponsor | IRCCS Azienda Ospedaliero-Universitaria di Bologna Academic / other |
| Locations | 1 site (Bologna) |
| Status | Recruiting |
| Started | April 21, 2021 |
| Main results expected | March 2030 |
| Study ends | April 2030 |
| Registry record updated | January 14, 2025 |
| Trial ID | NCT06774690 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults over 18 diagnosed with HCC or iCCA who are indicated for intra-arterial therapies.
✕Probably not a fit
Patients with metastasis outside the liver or those experiencing liver failure may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to identify the optimal conditions for positive outcomes in patients receiving intra-arterial therapy (IAT) for primary liver cancers, specifically Hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinoma (iCCA). Researchers will collect and analyze both retrospective and prospective data from participants at the IRCCS Azienda Ospedaliera Universitaria in Bologna. The study will evaluate clinical and radiological traits, including imaging assessments, to understand treatment responses and potential complications. The study expects to enroll approximately 3,300 participants over a five-year period.
Why it matters
Potential benefit: If successful, this study could enhance treatment strategies for liver cancer, leading to improved patient outcomes.
How similar studies have gone: While similar approaches have been explored, this study focuses on a comprehensive observational analysis, making it a novel contribution to the field.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * diagnosis of Hepatocellular carcinoma (HCC) or intrahepatic cholangiocarcinoma (iCCA) and clinical indication to receive or have already received one of the following treatments: * Trans-arterial embolization (TAE), * Transarterial chemoembolization (TACE), * Transarterial radioembolization (TARE) * Drug-eluting beads chemoembolization (DEB-TACE) * Age over 18 * To give informed consent Exclusion Criteria: * shunt of gastro intestinal arteries that cannot be embolized * metastasis spread outside of the liver * liver failure
Where it's running
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IRCCS Azienda Ospedaliero-Universitaria di Bologna
Bologna, Italy Recruiting
Study contacts
- Principal investigator: Cristina Mosconi, MD — IRCCS Azienda Ospedaliero-Universitaria di Bologna
- Study coordinator: Cristina Mosconi, MD
- Email: cristina.mosconi@aosp.bo.it
- Phone: 0039 3498496325
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.