Trials / Completed
CompletedNCT03845491
ASSIST Registry Studying Various Operator Techniques
ASSIST Registry to Assess the Procedural Success and Clinical Outcomes Associated With Various Operator Techniques for Mechanical Thrombectomy in Large Vessel Occlusions (LVO).
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 1,492 (actual)
- Sponsor
- Stryker Neurovascular · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this Registry is to assess the procedural success and clinical outcomes associated with various operator techniques for mechanical thrombectomy in large vessel occlusions (LVO).
Detailed description
ASSIST is a prospective, global, consecutive enrollment Registry of anterior circulation acute ischemic stroke patients with an LVO who undergo treatment with one of the interventional techniques using Stryker Neurovascular devices for the first pass. The purpose of this Registry is to assess the procedural success and clinical outcomes associated with various operator techniques for mechanical thrombectomy in large vessel occlusions (LVO) in the anterior circulation. Data will be collected on the use of Stryker market-released neurovascular mechanical access and mechanical thrombectomy devices that are commercially available or that may be approved for commercial use during the conduct of the Registry. This Registry will also collect data, including time-to-treatment and quality of life measures, to allow for subset analyses.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Mechanical Thrombectomy | Treatment of LVO with mechanical thrombectomy |
Timeline
- Start date
- 2019-01-24
- Primary completion
- 2022-04-11
- Completion
- 2023-01-25
- First posted
- 2019-02-19
- Last updated
- 2025-05-13
- Results posted
- 2025-05-13
Locations
72 sites across 11 countries: United States, Belgium, Canada, Czechia, France, Germany, Italy, South Korea, Spain, Switzerland, United Kingdom
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03845491. Inclusion in this directory is not an endorsement.