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Clinical Study of Targeted Cryoablation Therapy in the Treatment of Hepatic Carcinoma

Evaluating the Safety and Efficacy of Targeted Cryoablation Therapy in the Treatment of Hepatic Carcinoma

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02969096
Enrollment
30
Registered
2016-11-21
Start date
2016-10-31
Completion date
2018-12-31
Last updated
2016-11-21

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

Conditions

Liver Neoplasms

Brief summary

The purpose of this study is to evaluate the safety and efficacy of targeted cryoablation therapy for hepatic carcinoma.

Detailed description

A cryoprobe is inserted percutaneously under CT guidance into the targeted lesion. Patients undergo ablation using a freeze-thaw-freeze cycle lasting approximately 10-6-10minutes.

Interventions

PROCEDURETargeted Cryoablation Therapy

A cryoprobe is inserted percutaneously under CT guidance into the targeted lesion. Patients undergo ablation using a freeze-thaw-freeze cycle lasting approximately 6-10-6 or 8-10-8 minutes, respectively.

Sponsors

Shanghai University of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of liver cancer based on histology or the current accepted radiological measures. * Single Tumor size ≤5.0 cm in greatest diameter, or multiple tumor number≤3 and each tumor size≤ 3cm. * Life expectancy: Greater than 3 months. * Patients' liver function is Child-pugh A or B. * Ability to understand the study protocol and a willingness to sign a written informed consent document. * Unable to receive operative surgery.

Exclusion criteria

* Patients with other primary tumor except liver cancer. * History of coagulation disorders or anemia.

Design outcomes

Primary

MeasureTime frame
Rate of complete tumor ablationUp to 4 weeks post surgery

Secondary

MeasureTime frame
Adverse EventsUp to 4 weeks post surgery

Countries

China

Outcome results

None listed

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