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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07601464
Acronym
TERMOMIRNA
Enrollment
150
Registered
2026-05-22
Start date
2026-03-26
Completion date
2028-12-31
Last updated
2026-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatocarcinoma

Keywords

hepatocarcinoma, liver cancer, microRNA, thermoablation

Brief 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.

Interventions

None listed

Sponsors

IRCCS Azienda Ospedaliero-Universitaria di Bologna
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years

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.

Design outcomes

Primary

MeasureTime frameDescription
circulant microRNAAt baseline, at 24 hours, 1 month, 3 monthsmicro-RNAs differentially expressed between the complete response and disease residue groups
tissue microRNAAt baselinemicro-RNAs differentially expressed between the complete response and disease residue groups
Metabolomic analysisAt baseline, 24 hours, 1 month, 3 monthsIdentification of circulating metabolites differentially expressed between the complete response and disease residue groups

Secondary

MeasureTime frameDescription
Relapse Free Survival24 hours, 1 month, 3 months0-1
Overall Survival24 hours, 1 month, 3 months0-1
Hepatocarcinoma recurrence24 hours, 1 month, 3 monthsEcography

Countries

Italy

Contacts

CONTACTAndrea Boccatonda, MD
andrea.boccatonda@aosp.bo.it+39 0512143265

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 23, 2026