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Clinical Trial Summary

The goal of the study is to identify the maximum tolerated dose of endobronchial ultrasound-guided transbronchial injection (EBUS-TBNI) of cisplatin for Stage IV lung cancer.


Clinical Trial Description

Multiple studies have demonstrated feasibility and safety of delivering cisplatin directly into lung tumors using endobronchial ultrasound guided-transbronchial needle injection (EBUS-TBNI). This technique relies on the use of a bronchoscope with an integrated ultrasound transducer allowing real-time visualization of, and delivery of cisplatin into, tumors lying in proximity to the central airways. Prior work has utilized this technique to treat loco regional recurrence in a previously radiated field. The goal of the current study is to identify the initial dose for intratumoral cisplatin. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04311762
Study type Interventional
Source University of Vermont
Contact Stephanie Burns
Phone (802) 656-8307
Email stephanie.burns@uvmhealth.org
Status Recruiting
Phase Phase 1
Start date February 26, 2020
Completion date March 2023

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