The ReCAna for Lower ExtremIty Venous OBstructions and In-StEnt Restenosis Registry
NCT: NCT07529756 · NOT_YET_RECRUITING
Brief Summary
The goal of this observational study is to gather additional safety and performance (effectiveness) data on the device for the treatment of symptomatic lower extremity venous obstructions and occlusions. The main questions the study aims to answer are: * What is the observed rate of safety events through the 30-day follow-up? * What is the rate of technical success (acute procedural success) achieved at the index procedure? Participants already undergoing treatment with the Recana as part of their regular medical care will be followed for 1 year.
Frequently Asked Questions
What is The ReCAna for Lower ExtremIty Venous OBstructions and In-StEnt Restenosis Registry?
The ReCAna for Lower ExtremIty Venous OBstructions and In-StEnt Restenosis Registry is a clinical trial registered under NCT07529756. Current status: NOT_YET_RECRUITING.
What is the status of NCT07529756?
The current status of NCT07529756 (The ReCAna for Lower ExtremIty Venous OBstructions and In-StEnt Restenosis Registry) is: NOT_YET_RECRUITING.
When did The ReCAna for Lower ExtremIty Venous OBstructions and In-StEnt Restenosis Registry start?
The ReCAna for Lower ExtremIty Venous OBstructions and In-StEnt Restenosis Registry started on 2026-06.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.