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| Name | Class |
|---|---|
| Mirada Medical | UNKNOWN |
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A pre- and postablation scan will be made intraprocedurally to investigate the feasibility of intraprocedural ablation verification assessment using coregistration software
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Additional intraprocedural CT-scan | Experimental | Additional intraprocedural CT-scan |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Additional intraprocedural pre-ablation CT-scan | Diagnostic Test | In 20 patients, besides de regular post-RFA scan, a pre-RFA contrast enhanced dual phase CT-scan will be acquired to investigate the feasibility of quantitative ablation assessment. |
| Measure | Description | Time Frame |
|---|---|---|
| Feasibility of the use of co-registration software (>80%) | The proportion of patients in whom reliable co-registration of pre- and post-ablation CT images is feasible | 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| Inter and intra-observer variability | Inter- and intraobserver variability of CT-CT co-registration of determining the minimum ablation margin after thermal ablation for liver tumors | 1 year |
| The time that is required for CT-CT co-registration |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Leiden University Medical Center | Leiden | South Holland | 2333ZA | Netherlands |
No individual patiend data is shared with researchers.
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prospective, single blind, single-arm, phase II stud
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post-procedural an assessment will be done of the ablation completeness using registration software. The actual ablation verification will be done qualitatively by the treating physician.
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The time that is required for CT-CT co-registration
| 1 year |
| Quantitatively assessed ablation margin | Percentage of local recurrence per group as categorized according to ablation margin: <0mm, 0-5mm, >5mm | 1 year |