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Effect of Renal Denervation in End Staged Renal Disease With Resistant Hypertension

Effects of Catheter Based Renal Sympathetic Denervation on Resistant Hypertension in End Stage Renal Disease in Korea

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02346045
Enrollment
40
Registered
2015-01-26
Start date
2014-09-30
Completion date
2018-10-31
Last updated
2015-01-26

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

Conditions

Hypertension

Keywords

hypertension

Brief summary

A. Hypertension is a major cardiovascular risk factor and numerous treatment strategies have been developed to treat hypertension properly and reduce cardiovascular risk. B. However, there is a subgroup of hypertension which are resistant to treatment. 1. Resistant hypertension is associated to sympathetic hyperactivity 2. Renal sympathetic nerve is known to be associated with systemic sympathetic activity 3. According to research of recent years, catheter based renal sympathetic denervation is a safe and effective treatment modality to treat resistant hypertension C. Resistant hypertension is observed in end stage renal disease (ESRD) frequently. D. Sympathetic hyperactivity is observed in ESRD patients E. Catheter based renal sympathetic denervation is expected to improve resistant hypertension in ESRD patients F. The aim the present study is to evaluate the effects and safety of catheter based renal sympathetic denervation on resistant hypertension in ESRD

Interventions

In the experimental arm, Intervention is renal sympathetic denervation using Symplicity® system (Medtronic Ardian Inc, Mountain View, CA, USA) and antihypertensive medications previously prescribed 1. After femoral puncture guiding catheter is engaged in renal artery 2. Symplicity radiofrequency ablation catheter is inserted into renal artery and by circular sequence, from distal to proximal portion, ablation energy is applied to the wall of renal artery 3. 4-5 ablations are applied in each renal artery. In the sham comparator, intervention is renal angiogram and continue antihypertensive medications previuosly decribed

Sponsors

Daewoong Pharmaceutical Co. LTD.
CollaboratorINDUSTRY
Daiichi Sankyo Korea Co., Ltd.
CollaboratorINDUSTRY
Seoul St. Mary's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Patients who are under hemodialysis due to end stage renal disease * Patients who have resistant hypertension with office SBP \>160 mmHg) * Patients who are or over 18 years old. * Patients who submit informed consent

Exclusion criteria

* Known secondary hypertension patients * Patients who have renal artery which is not adequate for renal denervation 1. The main renal artery diameter \< 4 mm, or renal artery length \< 20 mm 2. The renal arteries into which stable catheter insertion is difficulty and which have hemodynamically or anatomically significant stenosis 3. The renal arteries who have undergone renal angioplasty * Patients who have history of myocardial infarction, unstable angina, syncope cerebrovascular insufficiency or extensive atherosclerotic disease with intravascular thrombosis, or unstable plaque * Type 1 Diabetes * Patients who have scheduled percutaneous coronary intervention (PCI) or operation within 6 months * Hemodynamically significant valvular heart disease in which blood pressure reduction may cause significant deterioration of patient's health. * Primary pulmonary hypertension * Patients who have the intracardiac defibrillator(ICD) or pacemaker which do not allow delivery of radiofrequency energy. * Patients who require continuous oxygen supply or mechanical ventilation for treatment of obstructive sleep apnea * Patients who have serious medical condition which can compromise the safety of the patients and the safety and integrity of the study. * Patients who have unresolved drug issue, alcoholism * Patients who lack ability to understand and follow the instruction the researcher * Patient who cannot follow up * Patients who are registered in other trial * Patients who are pregnant, nursing or planning to be pregnant

Design outcomes

Primary

MeasureTime frame
The change of office systolic blood pressure after renal denervation6 month

Secondary

MeasureTime frame
Change of office diastolic blood pressure6 month
change in ambulatory blood pressure monitroing(ABPM): mean systolic blood pressure(SBP)/diastolic blood pressure(DBP), mean heart rate(HR), BP variability6 month
Change in plasma norepinephrine6 months
Change in pulse wave velocity6 months

Countries

South Korea

Contacts

Primary ContactKiyuk Chang, MD, PhD
kiyuk@catholic.ac.kr+822-2258-1139

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026