NCT07166731Recruiting
High Coverage CARotid Stenting vs. Medical Management Alone to Prevent EmboliSm From symptomaTic Non-stenotic cARotid Disease (SyNC)
High Coverage CARotid Stenting vs. Medical Management Alone to Prevent EmboliSm From symptomaTic Non-stenotic cARotid Disease (SyNC) - CARESTAR
Source: ClinicalTrials.gov · Last updated 4 Mar 2026
Brief summary (registry, in English)
Goal is to analyse the clinical safety and efficacy of the CARESTO® heal Stent within standard clinical routine for the treatment of patients with symptomatic non-stenotic carotid disease (SyNC) and with high-risk plaque features for stroke recurrence compared to medical treatment alone with respect to the mid- and long-term clinical outcomes.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 536 (estimated)
- First submitted
- 7 Aug 2025
- Start date
- 1 Mar 2026
- Primary completion date
- 31 May 2032
- Lead sponsor
- Acandis GmbH
- Diseases
- Stroke
- NCT number
- NCT07166731
What you commit to
- Study type: Observational
- Planned participants: 536
- From 1 Mar 2026 to the primary completion date, 31 May 2032
- 1 site 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
- Patients in whom the stroke was likely caused by one of the following diseases:
- Small vessel disease
- Large vessel atherosclerotic disease ≥ 50%
- Cardioembolism
- Other known disease e.g. vasculitis
- Patients with blood coagulation disorders
- Patients with known hypersensitivity to nickel-titanium
- Patients who are allergic to heparin
- Any known conditions that affect life expectancy to less than 12 months
- Any known conditions associated with an increased risk of endovascular treatment
Other
- Patients with acute complete occlusion of the carotid artery in an emergency setting
- Incidence of acute infarcts in other vascular (i.e., not ipsilateral carotid) territories
- Predominantly calcified Plaques (≥50% calcified plaque components on CT-Angio)
- Patients presenting with intraluminal carotid thrombus (e.g. characterized by 'donut sign' on CTA)
- Patients with highly tortuous vessels (\>90°) which may prevent access or safe insertion of the stent
- Patients with post-CEA re-stenosis or post-CAS re-stenosis
- Patients in whom access to the carotid lesion is impossible or associated with an increased risk of procedural complications
- Patients with lesions in the ostium of the common carotid artery
- Patients not able to visit the outpatient clinic for annual follow-up
Who the study is looking for
- Patients diagnosed with acute ischemic stroke or acute retinal artery ischemia within the last two weeks related to symptomatic non-stenotic carotid disease (SyNC) and high-risk carotid plaque features
- Ipsilateral acute ischemic stroke must be determined by acute ischemic infarct on DWI or CT OR
- by neurological symptoms indicating ipsilateral cortical deficits consistent with ischemia in the territory of the internal carotid artery and after exclusion of a significant microangiopathy
- Acute retinal artery ischemia must be determined by ophthalmologic examination
- Patients with no other identifiable cause of stroke, evaluated using standard echocardiographic examinations to exclude cardiogenic or aortogenic sources of embolism
- Symptomatic non-stenotic carotid disease defined as one or more plaques in the ipsilateral internal carotid artery causing 10-49% luminal narrowing AND
- Presence of high-risk plaque features which must be determined through visual inspection on CTA or MRI (Ultrasound findings alone are insufficient; features must be confirmed by CTA or MRI to meet the criteria):
- Identification of at least two of the following characteristics Plaque thickness ≥ 3mm Irregular plaque surface Ulceration \<50% plaque calcification Lipid-rich necrotic core
- and/or identification of at least one of the following characteristics Intraplaque haemorrhage
- Presence of carotid web characterized as shelf-like/linear, smooth filling defects
- Plaque assessment including evaluation of the presence of high-risk features by routine imaging (CTA, MRI) confirmed by an independent CoreLab
- Signed Informed Consent Form
- Patient ≥ 18 years
- mRS ≤ 3 at time of randomisation
- Dual antiplatelet therapy (DAPT) according to standard of care before endovascular treatment
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Städtisches Klinikum Solingen Coordinator of this site? Confirm its status | Solingen | Germany | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.