Renal Denervation in End Stage Renal Disease Patients With Refractory Hypertension

NCT ID: NCT00753116

Last Updated: 2012-11-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-09-30

Study Completion Date

2009-12-31

Brief Summary

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The purpose of this this study is to investigate the clinical utility of renal denervation in the treatment of ESRD patients with refractory hypertension.

Detailed Description

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Conditions

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Kidney Failure, Chronic Renal Dialysis

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Renal Denervation with a catheter-based procedure

Disruption of the renal nerves with a catheter-based procedure

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Systolic blood pressure of 160 mmHg or greater
* On 3 or more antihypertensive medications
* On dialysis for more than 6 months

Exclusion Criteria

* Renal artery abnormalities
* Known secondary hypertension attributable to a cause other than sleep apnea
* MI, angina, CVA within 6 months
* Others
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Medtronic Vascular

INDUSTRY

Sponsor Role lead

Responsible Party

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Ardian Inc.

Locations

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Hennepin County Medical Center

Minneapolis, Minnesota, United States

Site Status

Countries

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United States

Other Identifiers

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TP-041

Identifier Type: -

Identifier Source: org_study_id