CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 81 enrolled
Drug / intervention
TransForm™ Occlusion Balloon Catheterdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01949779
NCT01949779N/ACompleted
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TransForm™ Occlusion Balloon Catheter Registry

Stryker Neurovascular·observational·Posted Sep 25, 2013·Updated Sep 6, 2019

In Brief

An observational study evaluating TransForm™ Occlusion Balloon Catheter for Intracranial Aneurysms. Completed, enrolled 81 participants across 7 sites in 2 countries.

Detailed 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

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsIntracranial Aneurysms
CountriesSpain, United States
Collaborators--

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedSep 25, 2013
Enrollment StartDec 1, 2013
Primary CompletionJan 1, 2015
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 12.8 years ago

Interventions

TransForm™ Occlusion Balloon Catheterdevice

TransForm™ Occlusion Balloon Catheter