Fact CheckerSign in

NCT05732727RecruitingPhase 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

Intensification of Blood Pressure Lowering Therapeutics Based on Diuretics Versus Usual Management for Uncontrolled Hypertension IN Patients With Moderate to Severe Chronic Kidney Disease: an Open Label, a Cluster Randomized Controlled, Phase 3 Trial

Source: ClinicalTrials.gov · Last updated 3 Aug 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
720 (estimated)
First submitted
8 Feb 2023
Start date
28 Mar 2023
Primary completion date
Mar 2029
Lead sponsor
University Hospital, Tours
NCT number
NCT05732727
EU CT number
2022-501494-39-00

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 720
  • From 28 Mar 2023 to the primary completion date, Mar 2029
  • 37 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Solid organ transplantation
  • Autosomal dominant polycystic kidney disease treated with Tolvaptan

Other illness

  • Major adverse cardiovascular event during the last three months: myocardial infarction, heart failure hospitalization, stroke
  • Current medical history of cancer requiring chemotherapy
  • Severe heart failure (NYHA III\_IV)

Lab values

  • Hyponatremia (\<130 mmol/L)
  • Dyskalemia (\<3,5 mmol/L or \>5,5 mmol/L)

Other

  • 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
  • Two or more diuretic agents (loop diuretic, thiazides and thiazide-like diuretics)
  • Mineralocorticoid receptor antagonists
  • Contraindication to diuretics involved in the algorithm
  • Cirrhosis Child B-C

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (37)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centre Hospitalier Universitaire D Angers
Coordinator of this site? Confirm its status
Angers Cedex 9FranceRecruiting
Centre hospitalier Universitaire de Bordeaux
Coordinator of this site? Confirm its status
BordeauxFranceRecruiting
Centre Hospitalier Regional Et Universitaire De Brest
Coordinator of this site? Confirm its status
Brest Cedex 2FranceRecruiting
Centre Hospitalier William Morey
Coordinator of this site? Confirm its status
Chalon Sur Saone CedexFranceRecruiting
Chu Gabriel Montpied
Coordinator of this site? Confirm its status
Clermont-FerrandFranceRecruiting
Centre Hospitalier Pasteur
Coordinator of this site? Confirm its status
Colmar CedexFranceRecruiting
Centre Hospitalier Universitaire Grenoble Alpes
Coordinator of this site? Confirm its status
Grenoble Cedex 9FranceRecruiting
Centre Hospitalier de Haguenau
Coordinator of this site? Confirm its status
HaguenauFranceRecruiting
Departmental Hospital Vendee
Coordinator of this site? Confirm its status
La Roche Sur Yon Cedex 9FranceRecruiting
Les Hopitaux De Chartres
Coordinator of this site? Confirm its status
Le CoudrayFranceRecruiting
Expansion Centres Hemodialyse Ouest
Coordinator of this site? Confirm its status
Le MansFranceRecruiting
Centre Hospitalier Du Puy
Coordinator of this site? Confirm its status
Le Puy-En-VelayFranceRecruiting
Centre Hospitalier Universitaire de Lille
Coordinator of this site? Confirm its status
LilleFranceRecruiting
Centre Hospitalier Universitaire de Limoges
Coordinator of this site? Confirm its status
LimogesFranceRecruiting
Hospices Civils De Lyon
Coordinator of this site? Confirm its status
Lyon Cedex 03FranceRecruiting
Assistance Publique Hôpitaux de Marseille
Coordinator of this site? Confirm its status
MarseilleFranceRecruiting
Centre Hospital Region Metz Thionville
Coordinator of this site? Confirm its status
Metz Cedex 03FranceRecruiting
Groupe Hospitalier de la Région de Mulhouse et Sud Alsace
Coordinator of this site? Confirm its status
MulhouseFranceRecruiting
Centre Hospitalier Universitaire de Nantes
Coordinator of this site? Confirm its status
NantesFranceRecruiting
Centre Hospitalier Universitaire De Nimes
Coordinator of this site? Confirm its status
Nimes Cedex 9FranceRecruiting
Centre Hospitalier Universitaire D Orleans
Coordinator of this site? Confirm its status
Orleans Cedex 2FranceRecruiting
Assistance Publique Hopitaux de Paris
Coordinator of this site? Confirm its status
ParisFranceRecruiting
Assistance Publique Hopitaux De Paris
Coordinator of this site? Confirm its status
Paris Cedex 18FranceRecruiting
Centre Hospitalier De Perpignan
Coordinator of this site? Confirm its status
Perpignan CedexFranceRecruiting
Centre Hospitalier Universitaire de Reims
Coordinator of this site? Confirm its status
ReimsFranceRecruiting
CHU De Rennes
Coordinator of this site? Confirm its status
Rennes Cedex 9FranceRecruiting
EXPANSION CENTRES HEMODIALYSE OUEST
Coordinator of this site? Confirm its status
RezeFranceRecruiting
Centre hospitalier de Roubaix
Coordinator of this site? Confirm its status
RoubaixFranceRecruiting
CHU De Rouen
Coordinator of this site? Confirm its status
Rouen CedexFranceRecruiting
Aub Sante
Coordinator of this site? Confirm its status
Saint-GregoireFranceRecruiting
EXPANSION CENTRES HEMODIALYSE OUEST
Coordinator of this site? Confirm its status
Saint-HerblainFranceRecruiting
Centre Hospitalier De Saint Malo
Coordinator of this site? Confirm its status
Saint-Malo CedexFranceRecruiting
Centre Hospitalier Universitaire de Saint Etienne
Coordinator of this site? Confirm its status
Saint-Priest-en-JarezFranceRecruiting
Les Hopitaux Universitaires de Strasbourg
Coordinator of this site? Confirm its status
StrasbourgFranceRecruiting
Centre Hospitalier Régional Universitaire de Tours
Coordinator of this site? Confirm its status
ToursFranceRecruiting
Centre Hospitalier de Valenciennes
Coordinator of this site? Confirm its status
ValenciennesFranceRecruiting
Centre Hospitalier Regional Universitaire De Nancy
Coordinator of this site? Confirm its status
Vandoeuvre Les NancyFranceRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.