Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Detachable Coils
Starting soon
Conditions studied: Arteriovenous Malformation, Gastrointestinal Bleed, Gastric Varices, Hemorrhoid, Pelvic Venous Disorders, Peripheral Aneurysms, Portal Vein Embolization, Type II Endoleak, Varicocele, Hemorrhage
In brief
The purpose of the Case-Specific Health Care Professional (HCP) Clinical Survey for Concerto Versa™ Detachable Coils, also known as the Concerto Versa HCP Clinical Assessment, is to collect early clinical data from HCPs to assess clinical safety and performance of the Concerto Versa™ Detachable Coils, when used in accordance with approved device labeling per the Instructions for Use (IFU). Data collected will generate clinical evidence to quantitatively assess clinical safety and device performance for the purpose of obtaining European Union Medical Device Regulation (EU MDR) approval.
Key facts
- Study ID
- NCT07639853
- Run by
- Medtronic Endovascular
- People needed
- 30
- Starts
- 2026-07-01
- Expected to finish
- 2026-11-01
- Last updated by the study team
- 2026-06-15
Who can join
Age: 22 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient treated with Concerto Versa™ Detachable Coil is age ≥ 22 years at the time of procedure.
- Use of Concerto Versa™ Detachable Coil in accordance with the device labeling.
- Reporting of case within 72 hours of index procedure.
Full record on ClinicalTrials.gov
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