# One-size-fits-all strategy in carotid artery treatment using CGuard stent, feasibility and clinical pilot study

**Authors:** Simone Balocco, Juan Rigla, Reimer Andresen, Christian Wissgott

PMC · DOI: 10.1186/s42155-025-00601-7 · CVIR Endovascular · 2025-10-16

## TL;DR

A pilot study shows that a one-size-fits-all 10-mm CGuard stent is safe and effective for treating carotid artery stenosis across different patient sizes.

## Contribution

This study introduces and validates a one-size-fits-all stent approach for carotid artery treatment, which is novel in vascular intervention.

## Key findings

- The CGuard stent achieved 100% technical success and 98.7% clinical success across all patient groups.
- No significant differences in outcomes were observed between groups with varying carotid artery diameters.
- Mid-term patency rates were high at 99% for ICA and 99.4% for ECA at one year.

## Abstract

Conventionally, the treatment of carotid artery disease customizes stents to the vessel diameter. The design of the CGuard stent and its nitinol shape memory allow for a wide operational range and minimal residual radial force. This pilot study assesses the feasibility and clinical outcomes of the 10-mm CGuard stent in a one-size-fits-all sizes protocol.

The study is a multicenter, prospective cohort study involving 226 consecutive patients with symptomatic or asymptomatic carotid artery stenosis, with an indication for revascularization. All patients received the 10-mm CGuard stent, irrespective of the carotid artery reference diameter, and were grouped into three categories based on the reference vessel diameter. Endpoints included procedural success and incidence of major adverse cardiovascular events (MACE) at 30 days and 1 year.

The study achieved 100% technical success, with an average residual stenosis of 8.41%. Clinical success was 98.7%. During in-hospital observation, one patient experienced a major ipsilateral stroke (0.4%), and two patients had transient ischemic attacks (TIAs) (0.8%). At the 30-day follow-up, there were one death and one case of re-occlusion which was asymptomatic. No differences between the three groups were found regarding technical or procedural success, residual stenosis, complications, TIAs, MACEs, or patency rates. No events occurred between the 30-day and 1-year follow-up, maintaining the MACE rate at 1.5%. ICA and ECA patency rates at 1 year were 99% and 99.4%, respectively, indicating mid-term treatment effectiveness.

This pilot study demonstrates that the one-size-fits-all approach using a 10-mm CGuard stent to treat carotid artery stenosis provides minimal residual radial force with optimal stent apposition. The one-size-fits-all approach with CGuard stent is feasible, safe, and effective. Further studies for confirmation are guaranteed.

The online version contains supplementary material available at 10.1186/s42155-025-00601-7.

## Linked entities

- **Diseases:** carotid artery stenosis (MONDO:0001612), stroke (MONDO:0005098), transient ischemic attacks (MONDO:0005264)

## Full-text entities

- **Diseases:** carotid artery stenosis (MESH:D016893), stenosis (MESH:D003251), carotid artery disease (MESH:D002340), TIAs (MESH:D002546), death (MESH:D003643), stroke (MESH:D020521)
- **Chemicals:** CGuard (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12528512/full.md

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Source: https://tomesphere.com/paper/PMC12528512