Skip to content

Noninvasive renal sympathetic denervation by high-intensity focused ultrasound (HIFU) in patients with refractory hypertension

Noninvasive renal sympathetic denervation by high-intensity focused ultrasound (HIFU) in patients with refractory hypertension

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-13003231
Enrollment
Unknown
Registered
2013-05-16
Start date
2013-05-20
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Hypertension

Interventions

HIFU Treatment Group:Renal sympathetic denervation by using the extracorporeal HIFU

Sponsors

The Second Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years, either sex; 2. the blood pressure can not reached the standard though have received and adhered to full doses of at least three antihypertensive drugs (include a diuretic), or can not tolerate the medications; 3. estimated glomerular filtration rate (eGFR) of >=45mL/min; 4. agrees to have the study procedure(s) performed and additional procedures and evaluations; 5. To be have competent and willing to provide written, informed consent to participate in this clinical study.

Exclusion criteria

Exclusion criteria: 1. pregnant woman, or planning to pregnant; 2. has a history or prior renal artery angioplasty; 3. has an implantable cardioverter defibrillator (ICD) or pacemaker; 4. has experienced MI or unstable angina pectoris within 6 months; 5. has experienced CVA within 6 months; 6. has hemodynamically significant valvular heart disease; 7. has respiratory failure requiring respiratory support; 8. has pyelolithiasis or ureteral calculus; 9. Obesity and renal arteries can not be clearly showed by the ultrasonic apparatus of Model-JC system; 10. with Type 1 diabetes; 11. has known, unresolved history of serious drug allergy; 12. have no legal capacity or legal capacity is limited; 13. currently enrolled in another investigational trial; 14. other situations that are considered not suitable for this clinical research.

Design outcomes

Primary

MeasureTime frame
Blood pressure;

Secondary

MeasureTime frame
Catecholamine hormones;Autonomic nerve reaction;Blood glucose;Glucose tolerance;Insulin release;Heart function;Glycated hemoglobin;

Countries

China

Contacts

Public ContactJing Huang
huangjing@cqmu.edu.cn+86 13508312022

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026