Status:

COMPLETED

Registry to Evaluate the ROX COUPLER in Patients With Resistant or Uncontrolled Hypertension

Lead Sponsor:

ROX Medical, Inc.

Conditions:

Hypertension

Blood Pressure, High

Eligibility:

All Genders

18-85 years

Phase:

PHASE3

Brief 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.

Eligibility Criteria

Inclusion

  • Diagnosis of resistant or uncontrolled hypertension must be made on the basis of current findings, medical history, and physical examination.

Exclusion

  • Any serious medical condition that may adversely affect the patient's safety, limit the subject's ability to participate in the registry, comply with follow-up requirements, or impact the scientific integrity of the study.

Key Trial Info

Start Date :

March 1 2014

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 5 2019

Estimated Enrollment :

83 Patients enrolled

Trial Details

Trial ID

NCT01885390

Start Date

March 1 2014

End Date

May 5 2019

Last Update

May 13 2019

Active Locations (4)

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Page 1 of 1 (4 locations)

1

ZNA Cardio Middelheim

Antwerp, Belgium, 2020

2

St. Antonius Ziekenhuis

Nieuwegein, Netherlands, 3435CM

3

East Sussex Healthcare NHS Trust

Eastbourne, United Kingdom, BN21 2UD

4

Queen Mary University of London

London, United Kingdom, EC1M 6BQ

Registry to Evaluate the ROX COUPLER in Patients With Resistant or Uncontrolled Hypertension | DecenTrialz