TransForm™ Occlusion Balloon Catheter Registry

NCT01949779 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 81

Last updated 2019-09-06

Study results available
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Summary

The primary objective of this registry is to collect real world data on the safety and performance of the TransForm™ Occlusion Balloon Catheter when used in current neurointerventional procedures

Conditions

  • Intracranial Aneurysms

Interventions

DEVICE

TransForm™ Occlusion Balloon Catheter

TransForm™ Occlusion Balloon Catheter

Sponsors & Collaborators

  • Stryker Neurovascular

    lead INDUSTRY

Eligibility

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

Timeline & Regulatory

Start
2013-12-31
Primary Completion
2015-01-31
Completion
2015-01-31

Countries

  • United States
  • 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 NCT01949779 on ClinicalTrials.gov