CREO - Microwave Ablation Feasibility Study
Sponsor: Banner Health • ClinicalTrials.gov ID: NCT07817147
Recruiting for Similar Conditions?
Sponsors are looking for patients like you. See if you qualify for compensated research studies.
Check Eligibility →Description
The goal of this study is to assess the overall success of energy delivery during treatment using the ultrasound guided microwave ablation device in patients with locally advanced, unresectable, or metastatic cancer. Secondly, this study aims to explore the procedural/clinical safety of treatment with the device and the antitumor effect following treatment with the device.
Interventions
-
EUS-Guided MWA Device
(Device)
The rationale of this study is to generate preliminary data on the functionality and safety of Creo's MicroBlate™ Fine device when used under EUS guidance. The results generated from this study will inform any decisions regarding subsequent pivotal trials and may support the integration of this approach into clinical practice for anatomically challenging tumors.
Eligibility criteria
Conditions
Locations
- Banner MD Anderson Cancer Center and Gateway Hospital — Gilbert, Arizona, United States
- Cedars Sinai — Los Angeles, California, United States
- Rush University Medical Center — Chicago, Illinois, United States
- Mayo Clinic Rochester — Rochester, Minnesota, United States
- University of Tennessee Medical — Knoxville, Tennessee, United States
- Memorial Hermann-Texas Medical Center — Houston, Texas, United States
- West Virginia University Medicine — Morgantown, West Virginia, United States
Partner with Nurenyx
Showcase your study to thousands of motivated patients matching your criteria.
Learn MoreOfficial Source
Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
View Official Record