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To Improve the Clinical Outcome of Ultrasound-guided Radiofrequency Ablation by NAVIRFA® Navigation System.

To Improve the Clinical Outcome of Ultrasound-guided Radiofrequency Ablation by NAVIRFA® Navigation System.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05818176
Enrollment
60
Registered
2023-04-18
Start date
2023-04-01
Completion date
2023-12-31
Last updated
2023-04-18

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

Conditions

Radiofrequency Ablation

Brief summary

Ultrasonic-guided radiofrequency ablation is the most common minimally invasive treatment for liver cancer. This study will use my country's self-developed intelligent ultrasonic navigation tool (NAVIRFA® Navigation System) to assist in the puncture of the needle during ablation, to observe the operation time, Whether the needle accuracy, ablation effect and complications are different from the traditional free-hand ultrasonic guidance technology.

Interventions

DEVICENAVIRFA® Navigation System

radiofrequency ablation by NAVIRFA® Navigation System.

DEVICEultrasound

radiofrequency ablation by ultrasound

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients with malignant liver tumors less than three centimeters in size who are expected to suffer radiofrequency tumor ablation in the hospital. 2. At least 20 years old.

Exclusion criteria

1. Patients with abnormal coagulation function and low platelets are not suitable for ablation therapy after evaluation by the trial host. 2. Those who are unable to accept computerized tomography and MRI examinations, such as poor renal function or contrast agent allergy, are not suitable for examination after the evaluation of the test host.

Design outcomes

Primary

MeasureTime frameDescription
required scan timeBefore ablation treatmentthe time required until start of the ablation (measured from the time of the first US scan to the start of the ablation).

Countries

Taiwan

Contacts

Primary ContactKai-Wen Huang, MD, PhD
fangyu0429@gmail.com+886-23123456

Outcome results

None listed

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