MicroNet-covered Stent System for Stroke Prevention in All Comer Carotid Revascularization
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- STATUS
- Recruiting
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- End date
- Jun 29, 2026
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- participants needed
- 550
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- sponsor
- John Paul II Hospital, Krakow
Summary
All-comer study of unselected patients suitable for carotid artery revascularization to evaluate the feasibility, efficacy and safety of first line endovascular revasculariztion using MicroNet covered stent (CGuard) in the treatment of consecutive symptomatic and increased-stroke-risk asymptomatic carotid lesions that require revascularization by Neurovascular Team decision.
Description
Independent investigator initiated, academic, single arm, open-label, non-randomized,
prospective, multicenter, multispecialty trial of CGuard routine use in all-comer population
of consecutive patients with symptomatic or increased-stroke-risk asymptomatic carotid
Increased-stroke-risk is defined as the following patient and/or lesion characteristics:
thrombus containing, documented progressive, irregular,
The main objective of this observational study is to evaluate (1) the periprocedural
feasibility and efficacy of CGuard stent system in the treatment of
The study hypothesis is that the novel CGuard MicroNet covered stent is safe and effective for a majority of consecutive patients considered to require carotid revascularization.
Details
| Condition | CAROTID ARTERY DISEASE, CAROTID ARTERY DISEASE |
|---|---|
| Age | 18years - 100years |
| Treatment | Carotid artery stenting |
| Clinical Study Identifier | NCT04271033 |
| Sponsor | John Paul II Hospital, Krakow |
| Last Modified on | 19 February 2024 |
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Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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