Chronic kidney disease (CKD) is a major public health issue worldwide. Hypertension is the first risk factor in patients with CKD for mortality, cardiovascular disease and end-stage renal disease. It's now well established that lowering blood pressure (BP) reduces renal and cardiovascular complications in this high-risk population. In the general population, in addition to lifestyle interventions, the strategy to initiate and escalate a BP-lowering drug treatment is well described. The drug therapies recommended to achieve optimal BP control in the general population are the following: blockers of the renin-angiotensin system (angiotensin-converting enzyme inhibitors (ACEi) or angiotensin receptor blockers (ARB)), diuretics (thiazides and thiazide-like diuretics), and calcium channel blockers. For patients with CKD, the guidelines advise to start the BP-lowering agent with ACEi or ARB, but then, there is no strong evidence to support the preferential use of any particular agent in controlling BP and the results of clinical trials are discordant. In the NephroTest cohort, a French cohort of patients with CKD stage 1 to 5, among 2015 patients, 1782 had hypertension, only 54% had a diuretic and 44% had uncontrolled hypertension. In this cohort, extracellular fluid (ECF) overload was an independent determinant of hypertension, uncontrolled hypertension and apparent treatment resistant hypertension. In the same cohort, ECF overload was independently associated with end-stage kidney disease and death. Our hypothesis is that patients with CKD and uncontrolled hypertension are fluid overloaded and that the second line of treatment after an ACEi or an ARB should be a diuretic. We hypothesize that a specific algorithm to lower BP in patients with moderate to severe CKD based on diuretics will be more effective in term of cardiovascular event, mortality and evolution to end-stage kidney disease as compared to standard of care.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
720
Antihypertensive algorithm based on diuretics agents
standard of care management for antihypertensive therapy intensification
Department of Nephrology, University Hospital of Angers
Angers, France
RECRUITINGDepartment of Nephrology, University Hospital of Bordeaux
Bordeaux, France
RECRUITINGAUB Santé foundation, Brest
Brest, France
RECRUITINGDepartment of Nephrology, University Hospital of Brest
Brest, France
End stage kidney disease
The primary endpoint is a time to event outcome, considering the following composite endpoint: * End stage kidney disease * eGFR decline of at least 40% * Cardiovascular events among myocardial infarction, heart failure, hospitalization and stroke * All cause mortality
Time frame: Up to 36 months
eGFR decline of at least 40%
The primary endpoint is a time to event outcome, considering the following composite endpoint: * End stage kidney disease * eGFR decline of at least 40% * Cardiovascular events among myocardial infarction, heart failure, hospitalization and stroke * All cause mortality
Time frame: Up to 36 months
Cardiovascular events
The primary endpoint is a time to event outcome, considering the following composite endpoint: * End stage kidney disease * eGFR decline of at least 40% * Cardiovascular events among myocardial infarction, heart failure, hospitalization and stroke * All cause mortality
Time frame: Up to 36 months
All cause mortality
The primary endpoint is a time to event outcome, considering the following composite endpoint: * End stage kidney disease * eGFR decline of at least 40% * Cardiovascular events among myocardial infarction, heart failure, hospitalization and stroke * All cause mortality
Time frame: Up to 36 months
Time to end-stage kidney disease
All components of the composite endpoint will be assessed separately
Time frame: Up to 36 months
Time to eGFR decrease of at leat 40%
All components of the composite endpoint will be assessed separately
Time frame: Up to 36 months
Time to the first cardiovascular event among myocardial infarction, heart failure, hospitalization and stroke
All components of the composite endpoint will be assessed separately
Time frame: Up to 36 months
All-cause mortality
All components of the composite endpoint will be assessed separately
Time frame: Up to 36 months
Change from baseline in blood pressure
Systolic and diastolic blood pressure at months 3 and 6 then every 6 months (home blood pressure monitoring and office blood pressure measurement),
Time frame: From baseline and up to 36 months
Proportion of patients with controlled blood pressure
Proportion of patients with controlled blood pressure at 2 years (PA\< 135/85mmHg with home blood pressure monitoring)
Time frame: 24 months
Change from baseline in glomerular filtration rate
Change from baseline in glomerular filtration rate estimated by CKD-EPI formula at months 3 and 6 then every 6 months
Time frame: From baseline and up to 36 months
Change from baseline in proteinuria (g/d) or proteinuria /creatinuria (g/g)
Change from baseline in proteinuria (g/d) or proteinuria /creatinuria (g/g) at months 3 and 6 then every 6 months
Time frame: From baseline and up to 36 months
Proportion of patients who used at least one diuretic
Time frame: Up to 36 months
Change from baseline in quality of life
Change from baseline in quality of life assessed by PROMIS-29 survey each year
Time frame: From baseline and up to 36 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Department of Nephrology, Hospital of Chalon-sur-Saône
Chalon-sur-Saône, France
RECRUITINGDepartment of Nephrology, Hospital of Chartres
Chartres, France
RECRUITINGDepartment of Nephrology, University Hospital of Clermont-Ferrand
Clermont-Ferrand, France
RECRUITINGDepartment of Nephrology, Hospital of Colmar
Colmar, France
RECRUITINGDepartment of Nephrology, University Hospital of Grenoble
Grenoble, France
RECRUITINGDepartment of Nephrology, Hospital of Haguenau
Haguenau, France
RECRUITING...and 30 more locations