PumaRx Registry Trial
Condition(s) studied
Investigational drug(s) / intervention(s)
RenovoCath®: Intra-arterial catheter delivery of chemotherapy agents for the collection of real-world data.
Study summary
This study is a multicenter, observational, post-marketing, registry study designed to track the safety and performance of the RenovoCath® device and assess survival outcomes in patients diagnosed with solid tumors who are treated with localized intra-arterial (IA) delivery of therapeutic agents to solid tumors using the RenovoCath® catheter.
Eligibility
Primary outcome measure(s)
- Safety of RenovoCath® as assessed by the number of participants experiencing adverse events related to the chemotherapy agents administered using RenovoCath. — From the time of the first treatment, until 30 days after the last treatment
Number of participants experiencing adverse events related to the chemotherapy agents administered using RenovoCath. - Performance of RenovoCath® as assessed by the number of participants experiencing adverse events related to the inter-arterial drug delivery procedure. — From the time of the first treatment, until 30 days after the last treatment
Track the performance of RenovoCath® in a real-world setting delivering a variety of therapeutic agents
Trial sites (3)
| Facility | City | Region | Status |
|---|---|---|---|
| Baptist Health South Florida | Coral Gables | Florida | Recruiting |
| University of Pennsylvania Medical Center | Pittsburgh | Pennsylvania | Recruiting |
| The University of Vermont Medical Center | Burlington | Vermont | Recruiting |
More RenovoRx trials in the USA
Other trials for the same condition
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 NCT06805461 on ClinicalTrials.gov ↗ ← All trials in the USA