TransForm™ Occlusion Balloon Catheter Registry

Completed

Conditions studied: Intracranial Aneurysms

In brief

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

Key facts

Study ID

NCT01949779

Run by

Stryker Neurovascular

People needed

81

Starts

2013-12-01

Expected to finish

2015-01-01

Last updated by the study team

2019-09-06

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject or legal representative is willing and has provided informed consent.
• Subject is scheduled to undergo a neurointerventional procedure that may include the use of the occlusion balloon catheter.
• Subject is over 18 years of age.

You may not qualify if…

• Subject's anatomy precludes safe delivery of the TransForm Occlusion Balloon Catheter.
• Subject's pregnant

Where it is running

• Desert Regional Medical Center — Palm Springs, California, United States
• Central Baptist Hospital — Lexington, Kentucky, United States
• University of Massachusetts Medical School — Worcester, Massachusetts, United States
• The Ohio State University Wexner Medical Center — Columbus, Ohio, United States
• West Virginia University — Morgantown, West Virginia, United States
• Medical College of Wisconsin — Milwaukee, Wisconsin, United States
• Hospital Universitario Donostia — Donostia / San Sebastian, Spain

Full record on ClinicalTrials.gov

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