Post-Market Clinical Follow-up Study of i-ED Coil and EDG v4 for Arteriovenous Malformation
NCT: NCT07687472 · NOT_YET_RECRUITING
Brief Summary
This is a prospective, multicenter, post-market clinical follow-up (PMCF) study to collect safety and performance data in patients with arteriovenous malformations (AVMs) who undergo endovascular coil embolization using the i-ED Coil and Electro Detach Generator v4 (EDG v4).
Frequently Asked Questions
What is Post-Market Clinical Follow-up Study of i-ED Coil and EDG v4 for Arteriovenous Malformation?
Post-Market Clinical Follow-up Study of i-ED Coil and EDG v4 for Arteriovenous Malformation is a clinical trial registered under NCT07687472. Current status: NOT_YET_RECRUITING.
What is the status of NCT07687472?
The current status of NCT07687472 (Post-Market Clinical Follow-up Study of i-ED Coil and EDG v4 for Arteriovenous Malformation) is: NOT_YET_RECRUITING.
When did Post-Market Clinical Follow-up Study of i-ED Coil and EDG v4 for Arteriovenous Malformation start?
Post-Market Clinical Follow-up Study of i-ED Coil and EDG v4 for Arteriovenous Malformation started on 2026-10-01.
Related Devices
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.