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Atorvastatin and Sympathetic Activity in Chronic Kidney Disease

Atorvastatin Reduces Sympathetic Activity in Patients With Chronic Kidney Disease

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01257009
Enrollment
10
Registered
2010-12-09
Start date
2009-08-31
Completion date
2010-07-31
Last updated
2010-12-09

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

Conditions

Hypertension, Stable Chronic Kidney Disease

Keywords

sympathetic activity, chronic kidney disease, atorvastatin, lipitor

Brief summary

Hypertensive chronic kidney disease (CKD) patients often have sympathetic hyperactivity which appears to contribute to the pathogenesis of hypertension and cardiovascular organ damage. Experimental studies and some clinical studies have shown that statin therapy can reduce central sympathetic activity. Blockade of the renin-angiotensin system (RAS), which is standard treatment for CKD, is known to lower sympathetic activity. The investigators hypothesize that adding a statin for 6 weeks to RAS blockade would further lower sympathetic activity in hypertensive stage 2-4 CKD patients. Methods: In ten stable CKD patients who are on chronic treatment with renin-angiotenis blockers, blood pressure and sympathetic activity (quantified by assessment of muscle sympathetic nerve activity, MSNA) will be assessed at baseline and 6 weeks after atorvastatin 20mg/day added. Ten other CKD patients will serve as time control and will be studied twice with an interval of 6 weeks without any change in medication, to quantify within subject reproducibility.

Detailed description

see above

Interventions

DRUGAtorvastatin

6 weeks treatment with atorvastatin and studying the effect of atorvastatin on sympathetic activity

Sponsors

UMC Utrecht
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* stable chronic kidney disease * Hypertension

Exclusion criteria

* renal replacement therapy * pregnancy * diabetes mellitus

Design outcomes

Primary

MeasureTime frame
Sympathetic activity4-6 weeks treatment

Countries

Netherlands

Outcome results

None listed

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