PREDICTT Clinical Trial: Prospective Evaluation Of Pressure-Enabled Delivery And Alterations In CT-Based Tumor-To-Normal Liver Ratio And Tumor Dose Using The Trinav Infusion System

ConditionsTumorLiver
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorM.D. Anderson Cancer Center

About this trial

This single-arm prospective study will compare CT-based tumor-to-normal ratio (TNR) measurements obtained using TriNav versus endhole microcatheters.

Eligibility criteria

Qualifiers

Patients over 18 years of age, of any race or sex, who have unresectable primary or metastatic tumors of the liver, and who are able to give informed consent

Patients must be eligible for Y90-radioembolization treatment, have an ECOG Performance Status score of ≤ 2, with a life expectancy of ≥ 3 months

At least one lesion ≥ 3.0 cm in shortest dimension

Negative pregnancy test in premenopausal women with an acceptable contraception

Disqualifiers

Contraindications to angiography and selective visceral catheterization

Evidence of potential delivery of greater than 30 Gy absorbed dose to the lungs with a single treatment session

CT based TNR of 3 or higher based on planning hybrid angioCT

Evidence of any detectable Tc-99m MAA flow to the stomach or duodenum, after application of established angiographic techniques to stop or mitigate such flow (eg, placing catheter distal to gastric vessels)

Trial design

Treatments tested in this trial

  • Y90 Microsphere Therapy

Treatment groups

20 Participants
are divided into 1 treatment group

Sponsors and collaborators

M.D. Anderson Cancer Center

Lead sponsor

TriSalus Life Sciences, Inc.

Collaborator