Efficacy Evaluation of Microwave Ablation Assisted by Diaphragm Hydrodissection for Hepatocellular Carcinoma and Comparative Analysis With Surgical

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorThe First Hospital of Jilin University

About this trial

The goal of this observational study is to evaluate the local efficacy and safety of hydrodissection-assisted microwave ablation for patients with hepatocellular carcinoma, and to compare its therapeutic outcomes with surgical resection for hepatocellular carcinoma. The main questions it aims to answer are:

Is hydrodissection-assisted microwave ablation safe and effective for treating hepatocellular carcinoma? How does the therapeutic effect of hydrodissection-assisted microwave ablation compare with surgical resection for hepatocellular carcinoma? Patients who receive either microwave ablation or surgical resection will Undergo a 2-year follow-up period.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Patients diagnosed with hepatocellular carcinoma who underwent diaphragm hydrodissectionassisted microwave ablation or surgical resection at our hospital. All patients were definitively diagnosed with hepatocellular carcinoma based on combined imaging and pathological findings.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Microwave Ablation Assisted by Diaphragm Hydrodissection

    Procedure/Surgery

    For subphrenic hepatocellular carcinoma treated with microwave ablation, ultrasound-guided injection of normal saline into the diaphragm is performed during ablation to establish a hydrodissection barrier and optimise lesion visualisation.

  • Surgical Resection

    Procedure/Surgery

    Patients with subphrenic hepatocellular carcinoma who undergo surgical resection are managed according to clinical diagnostic and therapeutic standards for hepatocellular carcinoma.

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: Hydrodissection-assisted microwave ablation cohort1 intervention
Group B: Surgical resection cohort1 intervention

Trial outcomes

Primary outcomes

1

Progression-free survival (PFS)

the time from initiation of treatment to disease progression or death.

Time frame
Up to 2 years after treatment

Secondary outcomes

1

Overall survival (OS)

the time from initiation of treatment to death, loss to follow-up, or last follow-up.

Time frame
Up to 2 years after treatment

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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