Stereotactic Liver Ablation Assisted With Intra-Arterial CT Hepatic Arteriography and Ablation Confirmation Software Assessment (STEREOLAB)

Recruiting now · Not applicable

Conditions studied: Liver Ablation, Hepatic

In brief

To achieve adequate tumor treatment coverage with sufficient minimal ablation margins, several steps are required: firstly, it is critical to define tumor boundaries and extent on intra-procedural CT image; secondly, accurate planning, targeting, and confirmation of ablation probe placement within the tumor; thirdly, the use of an intra-procedural imaging assessment method to evaluate minimal ablation margins is required to define whether sufficient minimal ablation margins was obtained or if additional ablation is needed. Taking all together, those factors points to the need of having a high-precision ablation methodology for intra-procedural planning, monitoring, and ablation margin assessment. Currently, such methods are only utilized in isolation and the benefit of a combined and standardized procedure workflow is unknown. Therefore, our primary goal of this single-arm clinical trial is to investigate the technical efficacy of a high-precision liver ablation technique comprised by stereotactic-guidance, CT during hepatic arteriography-based imaging analysis, and computer-based software assessment of ablation margins for the treatment of patients referred to ablation for the treatment of primary and secondary liver cancers.

Key facts

Study ID

NCT05361551

Run by

M.D. Anderson Cancer Center

People needed

50

Starts

2023-02-21

Expected to finish

2026-08-31

Last updated by the study team

2026-04-17

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients presenting with up to 5 colorectal liver metastasis measuring up to 5 cm who are referred to percutaneous ablation;
• Ability to completely cover the target tumor with at least a 5 mm ablation margin as determined per pre-procedure cross-sectional imaging;
• Distance to central bile ducts > 1 cm;
• Adequate glomerular filtration rate (GFR > 40) and no severe allergies to iodine contrast-media;
• Ability to understand and the willingness to sign written informed consent;
• Age > 18 years-old;
• Performance status 0-2 (Eastern Cooperative Oncology Group Classification [ECOG]);
• Expected survival > 12 months.

You may not qualify if…

• Use of other prior or concomitant local therapy at the target tumor(s).
• Active bacterial infection or fungal infection on the day of the ablation.
• Platelet < 50,000/mm3.
• INR > 1.5
• Patients with uncorrectable coagulopathy.
• Currently breastfeeding or pregnant (latter confirmed by serum pregnancy test).
• Physical or psychological condition which would impair study participation.
• ASA (American Society of Anesthesiologists) score of ≥ 4.
• Any other loco-regional therapies at the target lesion(s).
• Anatomical variations in the arterial-hepatic blood supply of the liver that preclude the use of CTHA imaging.

Where it is running

• M D Anderson Cancer Center — Houston, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

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