Study of Microwave Spherical Ablation and Traditional Microwave Ablation in Single Hepatocellular Carcinoma ≤5cm
Primary Purpose
Hepatocellular Cancer, Microwave Ablation, Microwave Spherical Ablation
Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
True circular microwave needle
Sponsored by
About this trial
This is an interventional treatment trial for Hepatocellular Cancer
Eligibility Criteria
Inclusion Criteria:
- Patient has high risk factors for HCC and was first diagnosed of HCC by by contrast-enhanced imaging (CECT/CEMRI/CEUS) and/or pathology ;
- Age range 18 to 75 years old;
- Single lesion with tumor diameter ≤5cm;
- Patient refuses surgery and determines to undergo microwave ablation
- Liver function Child Pugh A or B;
- No extrahepatic metastasis or portal invasion;
- Patient signs the informed consent.
Exclusion Criteria:
- The lesion has received treatment, including local ablation therapy and TACE therapy, etc;
- With portal vein invasion or extrahepatic metastases;
- Patient is with severe cardiopulmonary insufficiency.
- Patient is a pregnant or breastfeeding women.
- Patient is considered to be unsuitable to participate in the study
Sites / Locations
- Tianjin Third Central HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
MTA Group
MWA Group
Arm Description
Use true circular microwave needle for ultrasound-guided thermal ablation in MSA (microwave spherical ablation) group.
Use normal microwave needle for ultrasound-guided thermal ablation in MTA (microwave ablation) group.
Outcomes
Primary Outcome Measures
Comparison of progression-free survival between MSA and traditional MWA in HCC
Compare the time to tumor progression after therapy of MSA and traditional MWA in the treatment of single hepatocellular carcinoma with a diameter of ≤5 cm
Secondary Outcome Measures
Comparison of the overall survival of MSA and traditional MWA in HCC
Compare the time to of all-cause mortality after therapy of MSA and traditional MWA in the treatment of single hepatocellular carcinoma with a diameter of ≤5cm
Comparison of local progression rates of MSA and traditional MWA in HCC
Local progression was defined as new lesions with hyperenhancement in the arterial phase and low enhancement in the portal or delayed phase found adjacent to the ablation lesion (≤5 mm) during follow-up. Compare the local progression rates after therapy of MTA and traditional MWA in the treatment of single hepatocellular carcinoma with a diameter of ≤ 5 cm
Comparison of complete ablation rates of MSA and traditional MWA in HCC
Complete ablation was defined as the tumor showing no enhancement in three stages on contrast-enhanced imaging. Compare the rate of complete ablation after therapy of MTA and traditional MWA in the treatment of single hepatocellular carcinoma with a diameter of ≤5 cm
Comparison of the complications rate of MSA and traditional MWA in HCC
Compare the rate of the complications during and after the therapy of MSA and traditional MWA in the treatment of patients with single hepatocellular carcinoma with a diameter of ≤5cm
Full Information
NCT ID
NCT05361538
First Posted
April 29, 2022
Last Updated
December 11, 2022
Sponsor
Tianjin Third Central Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05361538
Brief Title
Study of Microwave Spherical Ablation and Traditional Microwave Ablation in Single Hepatocellular Carcinoma ≤5cm
Official Title
A Single-center, Prospective Randomized Controlled Study of Microwave Spherical Ablation and Traditional Microwave Ablation in the Treatment of Single Hepatocellular Carcinoma With a Diameter of ≤5cm
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 22, 2022 (Actual)
Primary Completion Date
June 1, 2023 (Anticipated)
Study Completion Date
June 1, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tianjin Third Central Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Comparison of the progression-free survival, overall survival, local progression rates, complete ablation rates and the complications rate of MSA and traditional MWA in the treatment of single hepatocellular carcinoma with a diameter of ≤5cm.
Detailed Description
HCC is a serious threat to the health of people,Early treatment of HCC results in a good prognosis for patients. Microwave ablation (MWA) is an important method for the treatment of early HCC. The traditional MWA technology has a long diameter of the ablation foci which is much larger than the transverse diameter, so in order to obtain a sufficient transverse diameter, the long diameter is often too large beyond the tumor boundary. That will cause too much normal liver tissue is unnecessarily damaged, especially for patients with severe liver cirrhosis or patients with liver cirrhosis who have undergone liver resection. In addition, it is easy to cause damage to adjacent vital tissues and organs. Changes in tissue properties during ablation affect the stability of the microwave field, resulting in unpredictable ablation shapes, which may cause omissions during tumor ablation, especially in multiple overlapping ablation, resulting in incomplete ablation, or increasing the risk of local tumor progression after treatment. Microwave spherical ablation (MSA) technology is a new MWA technology. With the help of temperature control technology, field control technology and wave control technology, a single needle can produce predictable spherical ablation lesions. Theoretically, MSA can improve the controllability of the ablation foci, which is suitable for the purpose of conformal ablation of large tumors in clinical practice, thereby minimizing the damage of local thermal ablation to liver tissue and adjacent important organs. However, there are few reports on the comparison of the therapeutic effect of MSA and traditional MWA. This study intends to conduct a prospective randomized controlled study based on the two mature microwave treatment methods of MSA and traditional MWA ablation to explore the effectiveness and safety of MSA in clinical application, providing evidence-based medical evidence for the clinical application of MSA.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Cancer, Microwave Ablation, Microwave Spherical Ablation, Prognosis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
MTA Group
Arm Type
Experimental
Arm Description
Use true circular microwave needle for ultrasound-guided thermal ablation in MSA (microwave spherical ablation) group.
Arm Title
MWA Group
Arm Type
No Intervention
Arm Description
Use normal microwave needle for ultrasound-guided thermal ablation in MTA (microwave ablation) group.
Intervention Type
Device
Intervention Name(s)
True circular microwave needle
Intervention Description
Use true circular microwave needle for thermal ablation
Primary Outcome Measure Information:
Title
Comparison of progression-free survival between MSA and traditional MWA in HCC
Description
Compare the time to tumor progression after therapy of MSA and traditional MWA in the treatment of single hepatocellular carcinoma with a diameter of ≤5 cm
Time Frame
6 to 12 months
Secondary Outcome Measure Information:
Title
Comparison of the overall survival of MSA and traditional MWA in HCC
Description
Compare the time to of all-cause mortality after therapy of MSA and traditional MWA in the treatment of single hepatocellular carcinoma with a diameter of ≤5cm
Time Frame
12 to 60 months
Title
Comparison of local progression rates of MSA and traditional MWA in HCC
Description
Local progression was defined as new lesions with hyperenhancement in the arterial phase and low enhancement in the portal or delayed phase found adjacent to the ablation lesion (≤5 mm) during follow-up. Compare the local progression rates after therapy of MTA and traditional MWA in the treatment of single hepatocellular carcinoma with a diameter of ≤ 5 cm
Time Frame
6 to 12 months
Title
Comparison of complete ablation rates of MSA and traditional MWA in HCC
Description
Complete ablation was defined as the tumor showing no enhancement in three stages on contrast-enhanced imaging. Compare the rate of complete ablation after therapy of MTA and traditional MWA in the treatment of single hepatocellular carcinoma with a diameter of ≤5 cm
Time Frame
1 month
Title
Comparison of the complications rate of MSA and traditional MWA in HCC
Description
Compare the rate of the complications during and after the therapy of MSA and traditional MWA in the treatment of patients with single hepatocellular carcinoma with a diameter of ≤5cm
Time Frame
immediately
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient has high risk factors for HCC and was first diagnosed of HCC by by contrast-enhanced imaging (CECT/CEMRI/CEUS) and/or pathology ;
Age range 18 to 75 years old;
Single lesion with tumor diameter ≤5cm;
Patient refuses surgery and determines to undergo microwave ablation
Liver function Child Pugh A or B;
No extrahepatic metastasis or portal invasion;
Patient signs the informed consent.
Exclusion Criteria:
The lesion has received treatment, including local ablation therapy and TACE therapy, etc;
With portal vein invasion or extrahepatic metastases;
Patient is with severe cardiopulmonary insufficiency.
Patient is a pregnant or breastfeeding women.
Patient is considered to be unsuitable to participate in the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiang Jing, MD
Phone
02284112323
Email
dr.jingxiang@aliyun.com
First Name & Middle Initial & Last Name or Official Title & Degree
Yan Zhou, MD
Phone
02284118101
Email
zhouyan2626@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiang Jing
Organizational Affiliation
Tianjin Third Central Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Tianjin Third Central Hospital
City
Tianjin
State/Province
Tianjin
ZIP/Postal Code
300170
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiang Jing, MD
Phone
02284112323
Ext
+86
Email
dr.jingxiang@aliyun.com
First Name & Middle Initial & Last Name & Degree
Yan Zhou, MD
Phone
02284118101
Ext
+86
Email
zhouyan2626@163.com
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Study of Microwave Spherical Ablation and Traditional Microwave Ablation in Single Hepatocellular Carcinoma ≤5cm
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