Trials / Completed
CompletedNCT02501148
A Multi-Center Study to Evaluate Acute Safety and Clinical Performance of Paladin® Carotid Post-Dilation Balloon System With Integrated Embolic Protection
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 106 (actual)
- Sponsor
- Contego Medical, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to assess the safety and clinical performance of Paladin System in patients with carotid artery stenosis.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | carotid artery stenting | Post-dilation of deployed self-expanding carotid stent with the Paladin Post-Dilation Balloon System with Integrated Embolic Protection |
Timeline
- Start date
- 2015-08-01
- Primary completion
- 2016-09-01
- Completion
- 2016-10-01
- First posted
- 2015-07-17
- Last updated
- 2022-11-21
Locations
5 sites across 1 country: Germany
Source: ClinicalTrials.gov record NCT02501148. Inclusion in this directory is not an endorsement.