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Recruiting Observational

Evaluation of Tissue and Circulating microRNA Profiles in Patients With Hepatocellular Carcinoma Subjected to Thermal Ablation

NCT07601464 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2026-03-26
Last updated
2026-05-22

Condition(s) studied

Hepatocarcinoma

Study summary

The main objectives of this research project concern the identification of microRNAs circulating and of serum metabolites predictive of treatment response in patients with early stage hepatocellular carcinoma undergoing locoregional treatment with thermoablation.

In addition, the molecular mechanisms involved in reprogramming will be identified metabolic via bioinformatics analysis and pretreatment liver biopsy analysis and analysis of screening on patient-derived primary lines for personalized therapy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
64 Years
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 * Diagnosis of hepatocarcinoma confirmed by radiology (LIRADS criteria/triphasic diagnostics) or by biopsy. * Indication for thermoablation treatment (for radiofrequency) based on the judgment of the hepatologist/surgeon. * Informed consent signed by the patient. Exclusion Criteria: * Presence of metastatic liver lesions of other origins. * History of liver transplant. * Severe, uncorrectable coagulopathy, contraindicating liver biopsy (where necessary) or ablative procedure. * Patient refusal to participate in the study or inability to obtain informed consent. * Pregnant women.

Primary outcome measure(s)

  • circulant microRNA — At baseline, at 24 hours, 1 month, 3 months
    micro-RNAs differentially expressed between the complete response and disease residue groups
  • tissue microRNA — At baseline
    micro-RNAs differentially expressed between the complete response and disease residue groups
  • Metabolomic analysis — At baseline, 24 hours, 1 month, 3 months
    Identification of circulating metabolites differentially expressed between the complete response and disease residue groups

Trial sites (1)

FacilityCityRegionStatus
IRCCS Policlinico di Sant'Orsola Bologna Emilia-Romagna Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07601464 on ClinicalTrials.gov ↗ ← All trials in Italy