Trials / Completed
CompletedNCT01885390
Registry to Evaluate the ROX COUPLER in Patients With Resistant or Uncontrolled Hypertension
ROX CONTROL HTN Registry: To Evaluate the ROX Coupler in Patients With Resistant or Uncontrolled Hypertension
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 83 (actual)
- Sponsor
- ROX Medical, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this registry is to evaluate the safety and performance of the ROX COUPLER in patients with treatment-resistant or uncontrolled hypertension.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | ROX COUPLER | The COUPLER will be used to create an anastomosis in the iliac region (between the iliac artery and vein). |
Timeline
- Start date
- 2014-03-01
- Primary completion
- 2019-05-05
- Completion
- 2019-05-05
- First posted
- 2013-06-25
- Last updated
- 2019-05-13
Locations
4 sites across 3 countries: Belgium, Netherlands, United Kingdom
Source: ClinicalTrials.gov record NCT01885390. Inclusion in this directory is not an endorsement.