A Non-Therapeutic study to assess the Functionality of the Kona Renal Denervation System in Subjects Undergoing Diagnostic Angiography

Not Applicable

Recruiting

• Conditions: Hypertension; Cardiovascular - Hypertension

• Registration Number: ACTRN12611000895987
• Lead Sponsor: Pacific Clinical Research Group

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2011-08-22
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

a.Subject is at least 18 years of age.
b.Subject is scheduled to undergo elective, diagnostic angiography.

Exclusion Criteria

a.Subject has a body weight > 150 kilograms.
b.Subject is pregnant, nursing or intends to become pregnant during the trial period.
c.Subject is currently enrolled in other potentially confounding research.
d.Subject has any condition that, at the discretion of the investigator, would preclude participation in the trial.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Assess the device-patient interface and renal artery targeting and tracking capability of the Kona Renal Denervation System (RDS) in patients who are undergoing diagnostic angiography via ultrasound[The ultrasound takes approximatley 5 minutes, and will occur after the routine angiography, just after the insertion of the Kona targeting catherter.]

Secondary Outcome Measures

Name	Time	Method
il[Nil]