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AcandiS Stenting of Intracranial STENosis - regisTry

NCT03902444 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2023-02-01

No results posted yet for this study

Summary

ASSISTENT is designed to collect comprehensive information on technical and clinical safety of the use of Credo® stent together with the NeuroSpeed® PTA balloon catheter in clinical practice in an open registry.

Conditions

  • Intracranial Stenosis

Interventions

DEVICE

Credo® Stent, NeuroSpeed® PTA balloon catheter

a self-expanding stent is used together with a PTA balloon catheter

Sponsors & Collaborators

  • Acandis GmbH

    lead INDUSTRY

Principal Investigators

  • Götz Thomalla, MD · Unversity Medical Center Hamburg-Eppendorf

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-31
Primary Completion
2025-03-31
Completion
2025-10-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03902444 on ClinicalTrials.gov