Post Marketing Study to Evaluate the NIMBUS Device

NCT03898960 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 54

Last updated 2025-04-25

Study results available
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Summary

A post-market study evaluating the NIMBUS Device in acute ischemic stroke patients with confirmed intracranial large vessel occlusion.

Conditions

  • Cerebral Stroke

Interventions

DEVICE

NIMBUS Device

NIMBUS Geometric Clot Extractor

Sponsors & Collaborators

  • Neuravi Limited

    lead INDUSTRY

Principal Investigators

  • René van den Berg, MD, PhD · Amsterdam UMC

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-10-30
Primary Completion
2022-02-15
Completion
2022-04-08

Countries

  • Germany
  • Sweden

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 NCT03898960 on ClinicalTrials.gov