Renal Artery DenervatIon Using Radial accesS in Uncontrolled HyperTensioN:Non Inferiority Study Comparing Safety and Efficacy of Radio Frequency Renal Denervation Using Iberis Renal Denervation System Via Radial Access Compared With Femoral

Status: Recruiting
Location: See all (11) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Non-inferiority, prospective, multi-center, international, post-market, randomized (1:1) clinical trial in patients with uncontrolled hypertension to compare the safety and efficacy of radio frequency renal denervation using Iberis Renal Denervation System via radial access compared with femoral access.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Patient ≥18 and ≤75 years old

• Persistent uncontrolled hypertension defined as the mean of three consecutive measurements of systolic office blood pressure \>150 mmHg and diastolic office blood pressure \>80 mmHg as well as ambulatory daytime systolic blood pressure ≥140 mmHg despite prescription of 2 to 5 anti-hypertensive drugs including an angiotensin-receptor blocker or an angiotensin-converting enzyme inhibitor in combination with a diuretic or calcium channel blocker

• Renal artery diameter ≥3 mm and ≤8 mm (to be assessed during the procedure)

• Patient can be treated according to the instructions for use (IFU)

• Patient eligible for TransFemoral Access and TransRadial Access

• Patient, who understands the trial requirements and the treatment procedures and provides written informed consent

Locations
Other Locations
France
Hôpital Saint André
RECRUITING
Bordeaux
Hôpital Jacques Cartier
RECRUITING
Massy
Centre Hospitalier de Pau
RECRUITING
Pau
Clinique Pasteur
RECRUITING
Toulouse
Germany
Zentrum für klinische Prüfungen in der Facharztzentrum Dresden Neustadt GbR
RECRUITING
Dresden
Asklepios Klinik Altona
RECRUITING
Hamburg
Saarland University Hospital
RECRUITING
Homburg
Johanniter-Krankenhaus Genthin-Stendal
RECRUITING
Stendal
Switzerland
University Hospital Basel
NOT_YET_RECRUITING
Basel
University & Hospital Fribourg
NOT_YET_RECRUITING
Fribourg
Cardiovascolare Istituto Cardiocentro Ticino
NOT_YET_RECRUITING
Lugano
Contact Information
Primary
Bradley S Hubbard, DVM
bshdvm@gmail.com
713-818-3188
Time Frame
Start Date: 2023-08-03
Estimated Completion Date: 2025-12-01
Participants
Target number of participants: 90
Treatments
Experimental: TransRadial access
Patients in this group are thus treated using a TRA approach
Active_comparator: TransFemoral Access
Patients in this group are thus treated using a TFA approach.
Related Therapeutic Areas
Sponsors
Leads: Shanghai AngioCare Medical

This content was sourced from clinicaltrials.gov