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Renal Sympathetic Denervation and Insulin Sensitivity (RENSYMPIS Study)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01785732
Acronym
RENSYMPIS
Enrollment
60
Registered
2013-02-07
Start date
2013-01-31
Completion date
2016-01-31
Last updated
2013-02-11

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

Conditions

Resistant Hypertension

Brief summary

Hypertension is a major risk factor for stroke and cardiovascular mortality. Catheter- based renal denervation causes substantial and sustained blood- pressure reduction in patients with resistant hypertension. The purpose of RENSYMPIS is to study the effects of renal denervation on: 1. Cardiovascular function 2. Metabolic factors 3. Inflammatory and endocrine factors 4. Coagulation 5. Sleep

Interventions

PROCEDURERenal Denervation

Sympathetic renal denervation via renal arteries

Sponsors

The Hospital District of Satakunta
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 69 Years
Healthy volunteers
No

Inclusion criteria

* Resistant Hypertension (systolic blood pressure \>160mmHg and 3 or more antihypertensive agents in use) * Age 30- 69 years * Written informed consent

Exclusion criteria

* Secondary hypertension * Pseudohypertension * Pregnancy * Renal insufficiency (GFR \<45ml/min) * Clinically significant stenotic valvular disease * Oral anticoagulation * CCS III-IV symptoms or CABG/PCI in previous 6 months * Prior stroke * Contrast agent allergy * inappropriate renal artery anatomy (\< 4mm diameter, \< 20mm length)

Design outcomes

Primary

MeasureTime frame
Office blood pressure2 years

Secondary

MeasureTime frame
Ambulatory blood pressure2 years
Insulin resistance2 years
Endothelial function2 years

Countries

Finland

Contacts

Primary ContactTuomas Paana, M.D.
tuomas.paana@satshp.fi+358 2 6277100
Backup ContactAntti Ylitalo, M.D. Ph.D
antti.ylitalo@satshp.fi+358 2 6277100

Outcome results

None listed

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