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Clinical research on application of transluminal renal arterial catheter radiofrequency ablation for blood pressure reduction in patients with drug-resistant essential hypertension

Clinical research on application of transluminal renal arterial catheter radiofrequency ablation for blood pressure reduction in patients with drug-resistant essential hypertension - Renal arterial catheter ablation for drug-resistant essential hypertension

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000010008
Enrollment
6
Registered
2013-02-11
Start date
2011-10-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Essential hypertension

Interventions

All participants undergo percutaneous transluminal catheter radiofrequency ablation in renal artery with 5Fr ablation catheter approved for treating cardiac arrhythmia. Initial 3 cases undergo 4W x 60

Sponsors

Department of Advanced Cardiovascular Therapeutics, Osaka University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Maintaining systolic blood pressure not less than 160mmHg (or 150mmHg with diabetes mellitus) under 3 or more kinds of anti-hypertensive medication. 2) Undergoing introduction about this study and give written informed consent.

Exclusion criteria

Exclusion criteria: 1) Renal anomaly or incompetency: Narrowing, previous renal angioplasty or stenting, or bifurcation. 2) Estimated glomerular filtration ratio less than 45mL/min. 3) Myocardial infarction, angina pectoris, or cerebrovascular disorder within recent 6 months. 4) Type 1 diabetes. 5) Secondary hypertension. 6) Prominent bleeding risk or coagulating disorder. 7) Diagnosed as any non-cardiovascular disease with less than 12 months more to live. 8) Current participants for any other clinical trial, excluding under extended observation period for evaluating approved drugs or materials. 9) Pregnancy. 10) Disqualified by any cardiologist for participating in this study.

Design outcomes

Primary

MeasureTime frame
1) No severe adverse effect after completion of protocol. 2) Lower blood pressure measures after 1, 3, 6, 12 months of operation than control with unchanged medication, or normalized pressure with reduced medication.

Countries

Japan

Contacts

Public ContactYuji Okuyama

Osaka University Graduate School of Medicine Department of Advanced Cardiovascular Therapeutics

yujicardiology@gmail.com

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026