At a glance
ClinicalIndex Comparison RecordN/ACompleted· 90 enrolled
Drug / intervention
Not specified
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.
A Single Center, Retrospective Study Evaluating the Use of the SoloPath® Sheath in Reducing Vascular and Bleeding Complications After Transcatheter Aortic Valve Implantation
In Brief
An observational study for Vascular Access Complication. Completed, enrolled 90 participants across 1 site.
Detailed Summary
This study is a retrospective, single center data collection to assess bleeding and vascular complications associated with TAVI when a SoloPath® Balloon Expandable TransFemoral Introducer is used for vascular access.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsVascular Access Complication
CountriesCanada
CollaboratorsMontreal Heart Institute
Timeline
N/ACompletedFinished
201520162017201820192020202120222023202420252026
Enrollment StartOct 2014
First PostedNov 2014
Primary CompletionMar 2015
Study CompletionApr 2015
TodayJul 2026
First PostedNov 21, 2014
Enrollment StartOct 1, 2014
Primary CompletionMar 1, 2015
Study CompletionApr 1, 2015
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 11.6 years ago