NCT04479020Completed
REcanalization of Distal Cerebral Vessels in Acute Stroke Using ApeRio®
Source: ClinicalTrials.gov · Last updated 6 Dec 2024
Brief summary (registry, in English)
The purpose of the REVISAR PMCF is to collect data in clinical practice of the APERIO® and APERIO® Hybrid(17) Thrombectomy Device, which are intended to restore blood flow in the neurovasculature by removing thrombus in patients experiencing ischemic stroke. Recanalization status will be assessed at the end of the procedure using the modified TICI (Thrombolysis in cerebral infarction) score.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 134 (actual)
- First submitted
- 2 Jul 2020
- Start date
- 1 Jul 2020
- Primary completion date
- 30 Jan 2024
- Lead sponsor
- Acandis GmbH
- Diseases
- Stroke
- NCT number
- NCT04479020
What you commit to
- Study type: Observational
- Participants enrolled: 134
- From 1 Jul 2020 to the primary completion date, 30 Jan 2024
- 11 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- pre stroke mRS ≥ 3
Other
- Any contraindication according to IFU
Who the study is looking for
- Any patient treated with the APERIO® or APERIO® Hybrid(17) Thrombectomy Device due to occlusion in distal vessel of the anterior and posterior circulation (postbifurcal MCA, ACA, PCA) according to IFU
- Age ≥ 18 years
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (11)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Schlosspark Klinik Charlottenburg Coordinator of this site? Confirm its status | Berlin | Germany | Unknown status |
| Universitätsklinikum Bonn Coordinator of this site? Confirm its status | Bonn | Germany | Unknown status |
| Universitätsklinikum Köln Coordinator of this site? Confirm its status | Cologne | Germany | Unknown status |
| Universitätsklinikum Düsseldorf Coordinator of this site? Confirm its status | Düsseldorf | Germany | Unknown status |
| Klinikum Fulda gAG Coordinator of this site? Confirm its status | Fulda | Germany | Unknown status |
| Universitätsmedizin Göttingen Coordinator of this site? Confirm its status | Göttingen | Germany | Unknown status |
| Universitätsklinikum des Saarlandes Coordinator of this site? Confirm its status | Homburg | Germany | Unknown status |
| Universitätsklinikum Magdeburg A.ö.R. Coordinator of this site? Confirm its status | Magdeburg | Germany | Unknown status |
| Johannes Wesling Klinikum Minden Coordinator of this site? Confirm its status | Minden | Germany | Unknown status |
| Klinikum der Universität München Coordinator of this site? Confirm its status | München | Germany | Unknown status |
| radprax Neurozentrum Solingen Coordinator of this site? Confirm its status | Solingen | Germany | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.