Intravascular Radiofrequency Ablation of Sympathetic Nerves for the Treatment of Hepatocellular Carcinoma

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age25-75
SponsorZhongda Hospital

About this trial

Patients who met the inclusion criteria were treated with endovascular radiofrequency ablation and desympathetic nerve surgery. After enrollment, endovascular radiofrequency ablation and desympathetic surgery were performed. After radiofrequency ablation, the safety and efficacy of follow-up treatment will be carried out every 1 month or so, including blood routine, liver and kidney function, tumor indicators, abdominal CT/magnetic resonance, etc.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Clinically or pathologically confirmed hepatocellular carcinoma (HCC)

Locally progressed or distant metastatic unresectable advanced HCC

Progressed after second-line therapy

Agree to participate in the study and sign the informed consent form

Disqualifiers

Not suitable for ablation surgery

Pregnant, lactating and planning to become pregnant

Orthostatic hypotension

Mixed liver cancer

Trial design

Design model

Single group

Treatments tested in this trial

  • endovascular radiofrequency ablation and desympathetic nerve surgery

    Procedure/Surgery

    endovascular radiofrequency ablation and desympathetic nerve surgery

Treatment groups

5 Participants
are divided into 1 treatment group
Group A: Intravascular Radiofrequency Ablation of Sympathetic Nerves GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

ORR

Objective Response Rate

Time frame
every month, up to 1 year

Secondary outcomes

1

PFS

Progression Free Survival

Time frame
every month, up to 1 year
2

DCR

disease control rate

Time frame
every month, up to 1 year

Other outcomes

Sponsors and contacts

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