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Cascade Clinical Data Collection Protocol

NCT04760925 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 112

Last updated 2022-10-04

No results posted yet for this study

Summary

This study is a multi-center, single arm, open label, retrospective and prospective clinical data collection of CascadeTM, Non-Occlusive Remodeling Net, in adults with intracranial aneurysms, demonstrating the effectiveness and safety of the CascadeTM in providing temporary assistance for coil embolization of intracranial aneurysms.

All consecutive eligible patients from all participating sites will be included in this clinical data collection. The relevant data of the coil embolization procedure will be collected via an eCRF system.

Peri procedural data on the coil embolization procedure as well as discharge, 30 days and at 3-6 months status will be collected.

Conditions

  • Intracranial Aneurysm

Interventions

DEVICE

CascadeTM, Non-Occlusive Remodeling Net

Temporary assistance device for coil embolization of intracranial aneurysms

Sponsors & Collaborators

  • Perflow Medical

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-03-05
Primary Completion
2021-11-03
Completion
2022-04-24

Countries

  • Bulgaria
  • Germany
  • Israel
  • Poland
  • Spain

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 NCT04760925 on ClinicalTrials.gov