Trials / Completed
CompletedNCT04416659
Flow Arrest Safety and Technical Success With Balloon Guide Catheters
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 52 (actual)
- Sponsor
- Medtronic Neurovascular Clinical Affairs · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this post-market registry is to assess technical efficacy and safety associated with the use of the BOSS Balloon Guide Catheter during neuro-vascular procedures while providing temporary arrest of blood flow.
Detailed description
This is a prospective, multi-center, non-randomized observational registry evaluating use of BOSS balloon guide catheters in patients diagnosed with an acute ischemic stroke due to large intracranial vessel occlusion.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Neuro-vascular access | Adjunctive device providing a conduit for retrieval device during thrombectomy |
Timeline
- Start date
- 2021-01-12
- Primary completion
- 2021-10-27
- Completion
- 2021-10-27
- First posted
- 2020-06-04
- Last updated
- 2022-04-28
Locations
9 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT04416659. Inclusion in this directory is not an endorsement.