Skip to main content
OpenTrials
Completed

NCT Number: NCT04420026

Study of Automatic Image Fusion of a CT Volume With Ultrasound During Percutaneous Ablation Treatment of Hepatic Tumors

The automatic fusion of the ultrasound with a cone-beam CT volume will guide the positioning of the electrodes, despite the visibility of the tumor in ultrasound, in patients treated with irreversible electroporation in the interventional radiology room at Avicenna Hospital for hepatocellular carcinoma (HCC). The objective is to evaluate the primary success rate of the automatic cone-beam CT fusion procedure and ultrasound, regardless of the tumor's visibility status in ultrasound.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Hepatocellular Carcinoma Adenocarcinoma Carcinoma Carcinoma, Hepatocellular Digestive System Diseases Digestive System Neoplasms Liver Diseases Liver Neoplasms Neoplasms Neoplasms by Histologic Type Neoplasms by Site Neoplasms, Glandular and Epithelial

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

SERROR

Bobigny, 93000, France

About this study

Percutaneous removal of hepatic tumours allows curative treatment using a range of techniques such as radiofrequency ablation, microwave, cryoablation or, more recently, irreversible electroporation. These treatments require the introduction of one or more electrodes into or around the areas to be treated. This insertion phase requires that the practitioner has a means of continuously visualizing the area to be treated and the position of the electrodes.

The reference modality for the treatment of hepatic tumours by ablation is ultrasound. The scanner is the conventional alternative recommended in case of invisibility of the target in ultrasound.

When the target is not clearly visible in ultrasound, advanced multimodal image fusion applications can allow the practitioner to overcome this difficulty. This fusion is made possible by tracking the movement of the ultrasound probe in relation to the patient using an electromagnetic navigation system, and by alignment between the ultrasound system and the fused volume.

This alignment can be done manually or automatically using a specific marker placed on the patient's skin, called an "Active Tracker".

The "INTERACT Active Tracker" functionality will also simplify the registration process by providing automatic pre-registration.

The purpose of this study is to prospectively evaluate the primary success of patients treated at Avicenna Hospital for HCC by irreversible electroporation using this fusion technique. The hypothesis of the study is that this image fusion makes it possible to improve the location of the lesions to be treated and to allow treatment by percutaneous ablation of lesions that are not very visible under ultrasound alone.

This study will also assess the time and accuracy savings when an automatic fusion solution between ultrasound and cone-beam (CB) CT is used, compared to manual alignment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age >18 years
  • Patient treated at Avicenna Hospital for HCC by irreversible electroporation (IRE)
  • Patient whose tumor treatment requires the use of fusion tools with CBCT imaging at the beginning of the procedure
  • Patients with a scheduled follow-up examination 1 month after the ablation procedure by irreversible electroporation (IRE)
  • Patient who has understood the information and agreed to participate in this research by signing the consent form
  • Patient affiliated to a social security system or entitled person

Exclusion criteria

  • Patients with a history of allergy to iodinated contrast material
  • Patients with MRI contraindications
  • Patients with a history of allergy to contrast material containing gadolinium
  • Pregnant or breastfeeding women
  • Patients under the protection of justice
  • Patients unable to understand research information in an informed manner
  • Participation in another interventional therapeutic trial

Treatment and study plan

Interact Active Tracker

Radiation

Interact Active Tracker, allowing the automation of the fusion between a CBCT and ultrasound imaging

Primary outcomes

  1. Evaluation of the primary success rate of percutaneous ablation treatment with IRE of hepatic tumors, as a function of the ultrasound visibility of the tumor, when using automatic CT cone-beam fusion and ultrasound

    Time frame: At 1 month on post-operative imaging

    Primary success is assessed on the control MRI or CT performed one month after the first IRE (Irreversible Electroporation) ablation procedure targeting a given tumor. It is defined by the absence of visible recurrence at 1 month on post-operative imaging. In the case of a partial response, a % of active tumor will be evaluated.

Secondary outcomes

  1. Evaluate the time savings when using "INTERACT Active Tracker" allowing automatic alignment of the CBCT volume with ultrasound

    Time frame: The day of the operation

    The ultrasound visibility of the tumor is evaluated by an ordered discrete variable defined as follows:

    0: Not identifiable with or without merging

    • identifiable with the help of fusion, tumor boundaries are poorly defined
    • identifiable with the help of fusion, the limits of the tumour are clearly visible
    • identifiable without fusion, tumor boundaries are poorly defined
    • identifiable without fusion, the limits of the tumour are clearly visible

  2. Evaluate the time saved by using "INTERACT Active Tracker" allowing automatic alignment of the CBCT volume with ultrasound compared to the manual alignment procedure performed on a series of patients treated when the new function was not available.

    Time frame: The day of the operation

    Time is measured from the moment the entire volume is loaded onto the ultrasound scanner. The stopwatch is stopped when the operator declares himself satisfied with the adjustment

  3. Evaluate the confidence gain associated with the use of ultrasound fusion.

    Time frame: The day of the operation

    The confidence gain associated with the use of ultrasound fusion is assessed by noting the number of non-visible or non-localizable tumors in ultrasound alone that can be identified through fusion.

  4. Evaluate the accuracy of the automatic alignment judged on the ultrasound measurement of the distance from the center of the target seen in ultrasound to that segmented on the pre-therapeutic pour Cone Beam Computed Tomography (CBCT).

    Time frame: The day of the operation

    The accuracy of the automatic alignment judged on the ultrasound measurement of the distance from the center of the target seen in ultrasound to that segmented on the pre-therapeutic CBCT is evaluated by comparison with the accuracy of the manual alignment recorded on a series of patients treated when the new function was not available

  5. Evaluate the percentage of procedures for which similarity points must be added due to an initial delay in automatic merging that the operator considers too long.

    Time frame: The day of the operation

    The percentage of procedures for which similarity points must be added due to an initial delay of the automatic merge considered too long by the operator is evaluated in comparison with the historical series (manual alignment, when the new function was not available).

  6. Evaluate the failure rate of the Interact Active Tracker automatic alignment.

    Time frame: The day of the operation

    If the operator is not satisfied with the automatic registration between the CBCT and ultrasound, the number of similarity point(s) to be placed and the time required to make this adjustment will be recorded

  7. Evaluate the secondary and third-party therapeutic effectiveness rate of the procedures.

    Time frame: The day of the operation

    The failure rate of the Interact Active Tracker automatic alignment is evaluated by the number of procedures where this function is not functional for any reason. Throughout the procedure, the number of times the operator will have to correct the alignment with new anatomical landmarks will be counted. Any failure of the automatic merge will be recorded.

  8. For incomplete responses, estimate the percentage of active tumour (enhanced by contrast material).

    Time frame: One month after the ablation

    The secondary and third-party therapeutic effectiveness rate of the procedures is defined by the number of cases in which two or three ablation procedures will be required to achieve a complete MRI response within one month of the last ablation session. For each tumour, the number of ablation procedures required to achieve a complete MRI response within one month of the last ablation session will be recorded. For patients requiring more than one treatment, only treatments performed over the duration of the study should be included.

  9. Assess the complication rate.

    Time frame: The day of the ablation

    The complication rate is evaluated by the Dindo-Clavian classification so complication will be recorded and classified

  10. Evaluate the global survival at 12 months

    Time frame: 12 months after the ablation

    Overall survival at 12 months. It will be collected by consulting medical records based on the recorded dates of the last visits, images...

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Collaborators

  • General Electric

Registry information

Official study title

Study of the Contribution of Automatic Image Fusion of a Cone-beam CT Volume With Ultrasound During Percutaneous Ablation Treatment of Hepatic Tumors

Acronym: IAT

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Jun 9, 2020
Registry last updated
Oct 4, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.