Neurovascular Product Surveillance Registry
Neurovascular Product Surveillance Registry is one of 9,000 trials in the TrialMatch dataset. Key details — Condition(s): Intracranial Aneurysm, Stroke, Ischemic; Status: Recruiting; Study type: Observational.
| Condition(s) | Intracranial Aneurysm, Stroke, Ischemic |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Summary | Post market surveillance registry |
| Who can participate | For MDT16056 and MDT17077 Inclusion Criteria: * Patient or legally authorized representative (LAR) provides authorization and/or consent per institution and geographical requirements * Patient has, or is intended to receive or be treated with, an eligible Medtronic product * Patient is consented within the enrollment window of the therapy received, as applicable * Patient is at least 18 years of age at time of enrollment. Exclusion Criteria: * Patient who is, or is expected to be inaccessible for follow-up * Patient with exclusion criteria required by local law * Patient is currently enrolled in or plans to enroll in any concurrent drug and/or device study that may confound results * Female patient who is known to be pregnant or is breastfeeding or wishes to become pregnant during particip |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | Medtronic Neurovascular Clinical Affairs |
| Locations | Buenos Aires, Argentina; Southport, Australia; Salzburg, Austria; Genk, Belgium; Ghent, Belgium; Beijing, China (+93 more sites) |
| Start date | 2016-12 |
| NCT ID | NCT02988128 |
| Official listing | https://clinicaltrials.gov/study/NCT02988128 |