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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05458791
Other study ID # SHA0010
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 1, 2022
Est. completion date January 2024

Study information

Verified date July 2022
Source Palo Alto Veterans Institute for Research
Contact Rajesh P Shah, MD
Phone 650-493-5000
Email rajesh.shah2@va.gov
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Patients are being asked to participate in a study to better determine blood flow going to tumors in the liver. They will undergo an embolization procedure in interventional radiology where the goal is to provide treatment directly into the liver tumor. These treatments are delivered into the blood vessels feeding the tumors. Improving these treatments relies on better understanding the blood flow into the tumor. By understanding how much blood flows into the tumors, the goal is to make sure there is the best chance of killing the tumor. The investigators are attempting to use a special type of CT scan during the procedure to determine the blood flow to the tumors.


Description:

Accurate liver imaging is critically important for the appropriate management of hepatocellular carcinoma (HCC) patients. The unique capability of the 4 dimensional (4D) CT system that combines CT and vascular imaging in real time has the great potential to provide physiologic and functional information to the operators to help guide therapy decisions during interventional procedures. However, the workflow, protocols and parameters have not been studied and optimized to support the use of perfusion techniques during interventional procedures. Efforts to reduce contrast and radiation doses associated with perfusion imaging to as low as reasonably achievable (ALARA) are also important steps to ensure patient safety while generating clinically meaningful images. Reducing radiation doses may be achieved by adjusting scan parameters, then applying reconstruction techniques to improve the image quality. The new generation of reconstruction algorithms, such as Model-Based iterative reconstruction, or deep-learning reconstruction algorithms (e.g. AiCE), simultaneously improve noise (lower dose) and enhances low contrast characteristics (less contrast). This pilot study aims to demonstrate the use of 4D CT system to acquire liver perfusion information to support the interventional procedure, and to derive as low as reasonably achievable (ALARA) dose levels and examine the robustness of reconstruction algorithms that generate clinically meaningful perfusion maps. The study will investigate the impact of different dose levels, and the robustness of reconstruction algorithms on CT perfusion maps. A successful study could allow for dissemination of these methods for use to the wider physician audience with an optimum ALARA dose levels. Furthermore, the potential knowledge gained from this study will further educate the medical community about the potential benefits of 4D CT intra-arterial CT perfusion as an adjunct imaging technique and may steer the direction for future larger scale trials and studies.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date January 2024
Est. primary completion date July 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Age > or = 18 years 2. primary or secondary liver tumor(s) 3. Trans-arterial chemoembolization (TACE) or trans-catheter radio embolization (TARE) approved by multidisciplinary tumor board 4. Tumor in an area without prior surgical or ablative therapy 5. At least 1 tumor greater than 1.5 cm in greatest diameter Exclusion Criteria: 6. Not eligible for TACE procedure. 7. Same additional exclusion criteria as aim 1 8. Any residual ethiodized oil accumulation in the liver 9. No prior IA treatment in the last year

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Intra-arterial Perfusion
All patients will undergo standard of care locoregional intra-arterial (IA) treatment for HCC. The procedure will take place utilizing fluoroscopic and CT guidance. Following catheterization of the femoral or radial artery, CT angiography of the hepatic circulation will be performed to define the hepatic vascular anatomy. Intra-arterial CT perfusion will be performed prior to IA treatment by the interventional radiologist to understand the dynamics of hepatic circulation or to manage the IA treatment strategy.

Locations

Country Name City State
United States VA Palo Alto Health Care System Palo Alto California

Sponsors (2)

Lead Sponsor Collaborator
Palo Alto Veterans Institute for Research Canon Medical Systems, USA

Country where clinical trial is conducted

United States, 

References & Publications (1)

Moawad AW, Szklaruk J, Lall C, Blair KJ, Kaseb AO, Kamath A, Rohren SA, Elsayes KM. Angiogenesis in Hepatocellular Carcinoma; Pathophysiology, Targeted Therapy, and Role of Imaging. J Hepatocell Carcinoma. 2020 Apr 23;7:77-89. doi: 10.2147/JHC.S224471. eCollection 2020. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Quantification of Parameters for Intra-arterial Perfusion Intra-arterial CT perfusion will be performed prior to IA treatment by the interventional radiologist to understand the dynamics of hepatic circulation or to manage the IA treatment strategy. 1 Day to 1 year
Secondary Impact of low dose radiation technique on intra-arterial perfusion parameters Evaluating low dose radiation on perfusion parameters 1 Day to 1 Year
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