Intra-procedural Spectral CT for Image-guided Embolization and Ablation in Interventional Oncology
1 other identifier
observational
30
1 country
1
Brief Summary
This is a pilot study to evaluate the feasibility, image quality, and procedural utility of a novel spectral CT technique using Canon Medical's 4D CT system during image-guided interventional oncology procedures
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Feb 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2025
CompletedFirst Submitted
Initial submission to the registry
March 17, 2025
CompletedFirst Posted
Study publicly available on registry
December 26, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2026
ExpectedDecember 26, 2025
March 1, 2025
1 year
March 17, 2025
December 18, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
CT image
Effective Dose and CTDI
Baseline
Secondary Outcomes (2)
number
Baseline
time
Baseline
Study Arms (3)
angiography mapping
Hepatocellular carcinoma (HCC) patients undergoing hepatic angiography mapping prior to TARE (N=10)
microwave ablation
percutaneous tumor ablation in patients receiving image-guided tumor ablation using MWA (n=10)
cryoablation
cryoablation (N=10) for primary liver (HCC) or primary kidney tumors (RCC)
Eligibility Criteria
patients with liver or kidney cancer being treated at VAPAHCS
You may qualify if:
- Age \> or = 18 years
- Tumor in an area without prior surgical or ablative therapy
- At least 1 tumor greater than 1.5 cm in greatest diameter
You may not qualify if:
- Not eligible for indicated procedure.
- BMI \> 35
- Prior surgery.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
VA Palo Alto Healthcare System
Palo Alto, California, 94304, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Sirish Kishore, MD
VA Palo Alto Health Care System
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 17, 2025
First Posted
December 26, 2025
Study Start
February 1, 2025
Primary Completion
February 1, 2026
Study Completion (Estimated)
September 1, 2026
Last Updated
December 26, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will not share