Trials / Completed
CompletedNCT01682057
A Multicenter Study to Evaluate the ROX Anastomotic Coupler System (ACS) In Patients With Severe Hypertension
A Prospective, Non-Randomized, Open Label, Multi-Center Study to Evaluate the ROX Anastomotic Coupler System (ACS) in Patients With Severe Hypertension
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 8 (actual)
- Sponsor
- ROX Medical, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the safety and performance of the ROX Anastomotic Coupler System (ACS) in patients with severe hypertension.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | ROX ANASTOMOTIC COUPLER SYSTEM (ACS) | The ROX Anastomic Coupler (ACS) will be used to create an arteriovenous fistula in the iliac region (between the iliac artery and vein). |
| DEVICE | ROX Anastomotic Coupler System (ACS) |
Timeline
- Start date
- 2011-10-01
- Primary completion
- 2013-03-01
- Completion
- 2013-03-01
- First posted
- 2012-09-10
- Last updated
- 2015-01-29
Locations
1 site across 1 country: Belgium
Source: ClinicalTrials.gov record NCT01682057. Inclusion in this directory is not an endorsement.