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Chinese Registry of Assisted Embolization for Ruptured Wide Necked Intracranial Aneurysm Using LVIS Stent

NCT02830386 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2016-07-12

No results posted yet for this study

Summary

This study aims to investigating the efficacy and safety of low profile visualized intraluminal support (LVIS) stents for the treatment of ruptured intracranial saccular aneurysms. The follow-up duration is 1 year.

Conditions

  • Self Efficacy
  • Medical Device Complication

Interventions

DEVICE

LVIS stent

Patients who meet the inclusion criteria will be treated with a low profile visualized intraluminal support (LVIS) stent with coils.

Sponsors & Collaborators

  • Changhai Hospital

    lead OTHER

Principal Investigators

  • Jianmin Liu, Doctor · Department of Neurosurgery, Changhai Hospital

Eligibility

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

Timeline & Regulatory

Start
2016-06-30
Primary Completion
2018-06-30
Completion
2018-11-30

Countries

  • China

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 NCT02830386 on ClinicalTrials.gov