REal-world Clinical evAulation of Medtronic NeurOVascular Products for Acute Ischemic Stroke (RECANOVA Registry)
Part of paid clinical trials in Flint, Michigan.
- Sponsor
- Medtronic Neurovascular Clinical Affairs
- Study ID
- NCT07599904
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Mechanical Thrombectomy — DEVICEIndex stroke procedure and follow-up visits up to 90 days post index procedure
Study Details
Post-Market Registry
Key Dates
- First listed
- May 20, 2026
- Start date
- Jul 31, 2026
- Status verified
- Jul 2026
- Primary completion
- Jul 31, 2031
- Completion
- Jul 31, 2031
Study Design
- Enrollment
- 1,500 participants (estimated)
Primary Outcome Measure
Evaluate device safety [ Time Frame: From Day 0 to 90 days post-procedure ]
Central Contacts
- Stephanie Salisbury612-979-7251
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| McLaren Flint Hospital | Flint | Michigan | 48532 | |
| Buffalo General Medical Center | Buffalo | New York | 14203 |
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