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NCT05128032: PEDIR

Pressure-enabled Delivery in Radioembolization (TriNav Study)

Active, enrolled NA Last updated 19 March 2026
What this trial tests

NA trial testing Standard microcatheter in Liver Cancer in 20 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
1 March 2022
Primary endpoint
1 June 2026
1 September 2026

Quick facts

Lead sponsorMassachusetts General Hospital
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposediagnostic
Enrollment20
Start date1 March 2022
Primary completion1 June 2026
Estimated completion1 September 2026
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Massachusetts General Hospital

Who can join

18 and older, any sex, with Liver Cancer or Hepatocellular Carcinoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of the study is to determine if the type of catheter used in the mapping procedure prior to radioembolization improves the delivery of radioactivity to tumor(s) in participants with liver cancer. The name of the devices involved in this study are: * Pressure Enabled Drug Delivery (PEDD)/TriNav Infusion System * Standard 2.4F microcatheter, not otherwise specified

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Liver Cancer

Currently open trials in the same condition.

Other Massachusetts General Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05128032.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing