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Single Session Combined Locoregional Therapies for Hepatocellular Carcinoma

Comparison of Single Session Transarterial Chemoembolization Combined With Microwave Ablation or Radiofrequency Ablation in Treatment of Hepatocellular Carcinoma: A Randomized Controlled Study

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02646137
Enrollment
50
Registered
2016-01-05
Start date
2015-01-31
Completion date
2023-12-31
Last updated
2018-01-09

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

Conditions

Liver Cancer

Brief summary

Hepatocellular carcinoma is the third most common cause of cancer-related mortality. In recent years, transarterial chemoembolization, radio frequency ablation and microwave ablation have been accepted as treatment modalities for patients with surgically unresectable hepatocellular carcinoma.

Detailed description

To compare between combination treatment with radiofrequency or microwave ablation followed by transarterial chemoembolization and performed in a single session.

Interventions

TACE exploits the preferential hepatic arterial supply of liver tumors for targeted delivery of chemotherapeutic agents followed by embolization or reduction in arterial flow using various types of particles

PROCEDURERadiofrequency ablation combined with TACE

Radiofrequency ablation (RFA) is an alternative therapy for HCC and liver metastases that can destroy a tumor by inducing thermal injury to the tissue through electromagnetic energy deposition

PROCEDUREMicrowave ablation combined with TACE

Microwave ablation (MWA) is an appealing alternative therapy for HCC in which a microwave antenna is placed directly into the tumor, emitting an electromagnetic wave which agitates water molecules in the surrounding tissue, producing friction and heat, thereby inducing cell death via coagulation necrosis

Sponsors

Tanta University
CollaboratorOTHER
Sherief Abd-Elsalam
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Child classification A or B. * serum albumin ≥ 3 gm/L. * serum bilirubin \< 2.5 mg/dL. * platelet count ≥70,000 mm3. * INR ≤ 1.6. * serum creatinine \< 2 mg/dl. * tumor size more than 4 cm and confined to one lobe of the liver.

Exclusion criteria

* Patients with portal vein thrombosis. * A technically inaccessible hepatic artery. * Metastatic HCC. * More than three lesions. * lesions in close proximity to the portal vein (PV),inferior vena cava (IVC) or gall bladder were excluded from the study.

Design outcomes

Primary

MeasureTime frameDescription
Number of patients with successful ablation3 monthsThe total number of patients with successful ablation

Countries

Egypt

Contacts

Primary ContactSherief M. Abd-Elsalam, Consultant
sherif_tropical@yahoo.com00201095159522

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026