LIFE-BTK (pivotaL Investigation of saFety and Efficacy of BRS treatment-Below The Knee) Randomized Controlled Trial

Brief description of study

The purpose of this research study is to evaluate the safety and performance of the Study Device for the treatment of narrowed arteries in critical limb ischemia (CLI), and compare the results to the current standard of care using a balloon, also called percutaneous transluminal angioplasty (PTA), the only approved therapy for the disease within United States.


Clinical Study Identifier: s20-00294
ClinicalTrials.gov Identifier: NCT04227899
Principal Investigator: Anvar Babaev.


If you are registered as a volunteer, please log in to contact the study team/express interest in this study.

Contact the research team to learn more about this study.

By clicking "Contact Research Team", your contact information will be sent securely to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.