MedTrace Logo

European eCLIPS™ Safety, Feasibility and Efficacy Study

NCT02607501 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2022-11-29

No results posted yet for this study

Summary

An open label, prospective, multicentre, single-arm, post marketing study evaluating the safety, technical feasibility, and efficacy of the eCLIPs™ Family of Products for the treatment of bifurcation intracranial aneurysms.

Conditions

  • Saccular Aneurysm
  • Intracranial Aneurysm

Interventions

DEVICE

Implant eCLIPs

Implant eCLIPs at target bifurcation aneurysm

Sponsors & Collaborators

  • Radboud University Medical Center

    collaborator OTHER

  • Evasc Medical Systems Corp.

    lead INDUSTRY

Principal Investigators

  • Joost DeVries, M.D. · Radboud University Medical Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-04-01
Primary Completion
2020-01-31
Completion
2021-09-30

Countries

  • Denmark
  • Germany
  • Netherlands

Study Locations

More Related Trials

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 NCT02607501 on ClinicalTrials.gov