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Clinical Trials in Australia / NCT02984566
Active, not recruiting Not applicable

Liver Ablative Radiotherapy Utilising Kilovoltage Intrafraction Monitoring (KIM)

NCT02984566 · tracked via the Priya Life Science Australia tracker
Phase
Not applicable
Started
2020-01-14
Last updated
2026-05-19

Condition(s) studied

Liver Cancer

Investigational drug(s) / intervention(s)

Kilovoltage Intrafraction Monitoring

Kilovoltage Intrafraction Monitoring: KIM is a novel intrafraction real-time tumour localization method. It involves a single gantry-mounted kV x-ray imager acquiring 2D projections of implanted fiducial markers. 3D positions are then reconstructed by maximum likelihood estimation of a 3D probability density function.

Study summary

Primary and secondary liver cancer patients will receive liver SABR with or without KIM intervention.

Eligibility

Sex
ALL
Min age
18 Years
Max age
85 Years
Healthy volunteers
No
Inclusion Criteria: * ECOG performance status 0-1 * Life expectancy \>6 months * Number of lesions: ≤ 3 * Lesion size : \< 10 cm for a single lesion (and up to 10 cm cumulative diameter for multiple lesions) * Child-Pugh A or B7 within 6 weeks prior to study entry * Unsuitable for RFA or resection or transplant * Distance from GTV to luminal structures (i.e., oesophagus, stomach, duodenum, small or large bowel) ≥ 10mm * All blood work obtained within 6 weeks prior to study entry with adequate organ function * May have had previous surgery, RFA or ethanol injection * Patient must have been discussed at multidisciplinary tumour board with consensus opinion for SBRT Exclusion Criteria: * HCC/cholangiocarcinoma with evidence of metastatic disease including nodal or distant metastases * Metastatic disease with complete liver disease response to first-line chemotherapy (i.e. no target for SBRT) * Previous radiation to the liver (including SIRTEX) * Untreated HIV or active hepatitis B/C * On systemic antineoplastic drug therapy within 7 days before inclusion * Pregnant or lactating women

Primary outcome measure(s)

Trial sites (4)

FacilityCityRegionStatus
Nepean Hospital Penrith New South Wales
Westmead Hospital Westmead New South Wales
Princess Alexandra Hospital Woolloongabba Queensland
Peter MacCallum Cancer Centre Melbourne Victoria

More University of Sydney trials in Australia

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT02984566 on ClinicalTrials.gov ↗ ← All trials in Australia