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Renal and Systemic Vascular Resistance in Chronic Kidney Disease (CKD)

The Role of Renal and Peripheral Vascular Resistance in Chronic Kidney Disease

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01380717
Acronym
RenVas
Enrollment
83
Registered
2011-06-27
Start date
2011-02-28
Completion date
2014-02-28
Last updated
2014-02-27

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

Conditions

Chronic Kidney Insufficiency, Hypertension, Vasodilation

Brief summary

Patients with reduced kidney function have a higher risk of heart disease and death. Studies have shown that blood vessels in patients with hypertension change with a decrease of lumen size and growth of the vessel wall. By treating patients with antihypertensive certain medication vessel lumen and walls normalize. Treating hypertension in patients with chronic kidney disease slows the progression of kidney function loss. The aim is to compare different degrees of antihypertensive medication in patients with chronic kidney disease and hypertension will slow the progression of kidney loss.

Interventions

DRUGBeta-blocker, ACE-inhibitor

Beta-blocker: 50- 100 mg 1-2 times a day. ACEi: 5-10 mg once a day

DRUGCalcium Channel Blockers, ACE-Inhibitor

Calcium Channel Blockers: 5-10 mg a day. ACEi: 5-10 mg a day

Sponsors

University of Aarhus
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* eGFR 15-60 ml/min for at least 3 months * Blood pressure \> 130 mmHg systolic og \>80 mmHg diastolic (patients without antihypertensive treatment or in treatment with Beta-blockers, ACEi, ARBs or CCB not in maximum dosi). * Blood pressure \< 130 mmHg systolic og \< 80 mmHg diastolic (patients receiving Beta-blockers, ACEi, ARBs og CCB). * Fertile women using safe contraceptives

Exclusion criteria

* Ultrasound verified Polycystic Kidney Disease (ADPKD) * Claustrophobia (MRi scan). * Contraindications to MRi. * Pregnancy or wish to become pregnant in the study period. * Nephrotic syndrome with gross edema. * Known allergy to any study medication. * Blood pressure \< 130 mmHg systolic or \< 80 mmHg diastolic without antihypertensive treatment. * Blood pressure \> 130 mmHg systolic or \> 80 mmHg diastolic and in maximum dosages of all three Beta-blockers, ACEi (ARBs) and CCB.

Design outcomes

Primary

MeasureTime frame
Change in glomerular filtration rate between the two treatment arms.Measured at baseline and after 18 months of treatment

Secondary

MeasureTime frame
Changes in glomerular filtration rate stratified after changes in pulse wave velocity, renal vascular resistance and forearm minimal resistance at baseline and after 18 months of treatment.18 months

Countries

Denmark

Outcome results

None listed

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