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Recruiting Phase 3

Intensification of Blood Pressure Lowering Therapeutics Based on Diuretics Versus Usual Management for Uncontrolled Hypertension IN Patients With Moderate to Severe Chronic Kidney Disease

NCT05732727 · tracked via the Priya Life Science France tracker
Phase
Phase 3
Started
2023-03-28
Last updated
2026-08-03

Condition(s) studied

Chronic Kidney Disease(CKD)Uncontrolled Hypertension

Investigational drug(s) / intervention(s)

Antihypertensive algorithmStandard of care

Antihypertensive algorithm: Antihypertensive algorithm based on diuretics agents

Standard of care: standard of care management for antihypertensive therapy intensification

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Male or female \>=18 years with a clinical frailty score ≤5 for patient aged over 80 * Advanced or moderate chronic kidney disease (eGFR 15 to 44.9 mL/min/1.73m² using CKD-EPI formula) * Arterial hypertension treated with at least one blood pressure lowering drug therapy among blockers of the renin-angiotensin system (ACEi or ARB), at the maximal posology tolerated by the patients stable since at least one month. Other blood pressure lowering drug therapies are tolerated in combination with or in the event of intolerance to ACE inhibitors or ARBs. * Uncontrolled office BP * Uncontrolled office BP (\>140 and/or 90 mmHg) confirmed by home blood pressure monitoring (\>135 and/or 85 mmHg) or Day-time Ambulatory Blood Pressure Monitoring * Participant covered by or entitled to social security * Written informed consent obtained from the participant Exclusion Criteria: * Patient following any measures of legal presentation * Pregnant or breastfeeding woman * woman of childbearing without a highly effective contraceptive measure (combined or progestogen-only hormonal contraception associated with inhibition of ovulation, intrauterine device or intrauterine hormone-releasing system) * Clinical signs of hypovolemia * Symptomatic orthostatic hypotension * Hyponatremia (\<130 mmol/L) * Dyskalemia (\<3,5 mmol/L or \>5,5 mmol/L) * Major adverse cardiovascular event during the last three months: myocardial infarction, heart failure hospitalization, stroke * Current medical history of cancer requiring chemotherapy * Solid organ transplantation * Two or more diuretic agents (loop diuretic, thiazides and thiazide-like diuretics) * Mineralocorticoid receptor antagonists * Autosomal dominant polycystic kidney disease treated with Tolvaptan * Contraindication to diuretics involved in the algorithm * Severe heart failure (NYHA III\_IV) * Cirrhosis Child B-C

Primary outcome measure(s)

  • End stage kidney disease — Up to 36 months
    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
  • eGFR decline of at least 40% — Up to 36 months
    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
  • Cardiovascular events — Up to 36 months
    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
  • All cause mortality — Up to 36 months
    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

Trial sites (40)

FacilityCityRegionStatus
Department of Nephrology, University Hospital of Angers Angers France Recruiting
Department of Nephrology, University Hospital of Bordeaux Bordeaux France Recruiting
AUB Santé foundation, Brest Brest France Recruiting
Department of Nephrology, University Hospital of Brest Brest France Recruiting
Department of Nephrology, Hospital of Chalon-sur-Saône Chalon-sur-Saône France Recruiting
Department of Nephrology, Hospital of Chartres Chartres France Recruiting
Department of Nephrology, University Hospital of Clermont-Ferrand Clermont-Ferrand France Recruiting
Department of Nephrology, Hospital of Colmar Colmar France Recruiting
Department of Nephrology, University Hospital of Grenoble Grenoble France Recruiting
Department of Nephrology, Hospital of Haguenau Haguenau France Recruiting
Department of Nephrology, Departemental Hospital of Vendée La Roche-sur-Yon France Recruiting
ECHO Santé Association, Le Mans Le Mans France Recruiting
Department of Nephrology, Hospital of Le Puy en Velay Le Puy-en-Velay France Recruiting
Department of Nephrology, University Hospital of Lille Lille France Recruiting
Department of Nephrology, University Hospital of Limoges Limoges France Recruiting
AUB Santé foundation, Lorient Lorient France Recruiting
Department of Nephrology, University Hospital of Lyon Lyon France Recruiting
Department of Nephrology, University Hospital of Marseille Marseille France Recruiting
Department of Nephrology, Regional Hospital of Metz Metz France Recruiting
Department of Nephrology, Régional Hospital of Mulhouse Mulhouse France Recruiting
Department of Nephrology, University Hospital of Nantes Nantes France Recruiting
ECHO Santé Association, Nantes Nantes France Recruiting
Department of Nephrology, University Hospital of Nîmes Nîmes France Recruiting
Department of Nephrology, Hospital of Orléans Orléans France Recruiting
Department of Nephrology, European Hospital Georges Pompidou, AP-HP Paris France Active Not Recruiting
Department of Nephrology, Necker Hospital, AP-HP Paris France Recruiting
Department of Nephrology, Bichat Hospital, AP-HP Paris France Recruiting
Department of Nephrology, Tenon Hospital, AP-HP Paris France Active Not Recruiting
Department of Nephrology, Hospital of Perpignan Perpignan France Recruiting
Department of Nephrology, University Hospital of Reims Reims France Recruiting
Department of Nephrology, University Hospital of Rennes Rennes France Recruiting
Department of Nephrology, Hospital of Roubaix Roubaix France Recruiting
Department of Nephrology, University Hospital of Rouen Rouen France Recruiting
Department of Nephrology, University Hospital of Saint Etienne Saint-Etienne France Recruiting
ECHO Santé Association, Saint Herblain Saint-Herblain France Active Not Recruiting
Department of Nephrology, Hospital of Saint Malo St-Malo France Recruiting
Department of Nephrology, Hospital of Strasbourg Strasbourg France Recruiting
Department of Nephrology, University Hospital of Tours Tours France Recruiting
Department of Nephrology, Hospital of Valenciennes Valenciennes France Recruiting
Department of Nephrology, University Hospital of Nancy Vandœuvre-lès-Nancy France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05732727 on ClinicalTrials.gov ↗ ← All trials in France