NCT07815054

Brief Summary

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.

Trial Health

65
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
37mo left

Started Oct 2026

Typical duration for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 7, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 11, 2026

Completed
20 days until next milestone

Study Start

First participant enrolled

October 1, 2026

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2028

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2029

Last Updated

September 11, 2026

Status Verified

September 1, 2026

Enrollment Period

2 years

First QC Date

September 7, 2026

Last Update Submit

September 7, 2026

Conditions

Keywords

Hepatocellular Carcinomamicrowave ablationProgression-Free SurvivalOverall SurvivalDiaphragm Hydrodissection

Outcome Measures

Primary Outcomes (1)

  • Progression-free survival (PFS)

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

    Up to 2 years after treatment

Secondary Outcomes (1)

  • Overall survival (OS)

    Up to 2 years after treatment

Study Arms (2)

Hydrodissection-assisted microwave ablation cohort

Patients with hepatocellular carcinoma receiving hydrodissection-assisted microwave ablation under routine clinical care. No study-specific intervention will be assigned by researchers.

Procedure: Microwave Ablation Assisted by Diaphragm Hydrodissection

Surgical resection cohort

Patients with hepatocellular carcinoma receiving surgical resection under routine clinical care. No study-specific intervention will be assigned by researchers.

Procedure: Surgical Resection

Interventions

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.

Hydrodissection-assisted microwave ablation cohort

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

Surgical resection cohort

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Carcinoma, Hepatocellular

Condition Hierarchy (Ancestors)

AdenocarcinomaCarcinomaNeoplasms, Glandular and EpithelialNeoplasms by Histologic TypeNeoplasmsLiver NeoplasmsDigestive System NeoplasmsNeoplasms by SiteDigestive System DiseasesLiver Diseases

Central Study Contacts

dezhi Zhang Associate Chief Physician, MD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Chief Physician,Abdominal Ultrasound Department

Study Record Dates

First Submitted

September 7, 2026

First Posted

September 11, 2026

Study Start

October 1, 2026

Primary Completion (Estimated)

September 30, 2028

Study Completion (Estimated)

September 30, 2029

Last Updated

September 11, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will not share