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HydroCoil Cerebral Aneurysm Treatment Trial

NCT01195129 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 215

Last updated 2014-12-12

No results posted yet for this study

Summary

The study will compare clinical and angiographic outcomes in patients receiving Hydrocoil aneurysm treatment versus patients receiving non-HydroCoil aneurysm treatment.

Conditions

  • Intracerebral Aneursym

Interventions

DEVICE

MicroVention Hydrogel coil

Micro Vention Hydrogel Coils

DEVICE

Non-hydrogel coils

Cerecyte or bare platinum coils

Sponsors & Collaborators

  • Microvention-Terumo, Inc.

    collaborator INDUSTRY

  • University of Virginia

    lead OTHER

Principal Investigators

  • Avery J Evans, MD · University of Virginia

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-12-31
Primary Completion
2013-04-30
Completion
2015-06-30

Countries

  • United States

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 NCT01195129 on ClinicalTrials.gov