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

Primary Purpose

Chronic Kidney Disease(CKD), Uncontrolled Hypertension

Status
Not yet recruiting
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Antihypertensive algorithm
Standard of care
Sponsored by
University Hospital, Tours
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Kidney Disease(CKD)

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Male or female >=18 years and <80 years of age 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. Uncontrolled office BP (>140 and/or 90 mmHg) confirmed by home blood pressure monitoring (>135/85 mmHg) 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 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

Sites / Locations

  • Department of Nephrology, University Hospital of Tours

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Experimental group

Control group

Arm Description

Antihypertensive algorithm based on diuretics agents : the clinicians will adjust the drug therapy according to the antihypertensive algorithm based on diuretics agents.

Standard of care : the clinicians will adapt the antihypertensive strategy according to his own standard of care which can be pharmacological or non-pharmacological therapies.

Outcomes

Primary Outcome Measures

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
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
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
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

Secondary Outcome Measures

Time to end-stage kidney disease
All components of the composite endpoint will be assessed separately
Time to eGFR decrease of at leat 40%
All components of the composite endpoint will be assessed separately
Time to the first cardiovascular event among myocardial infarction, heart failure, hospitalization and stroke
All components of the composite endpoint will be assessed separately
All-cause mortality
All components of the composite endpoint will be assessed separately
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),
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)
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
Change from baseline in proteinuria (g/d) or proteinuria /creatininuria (g/g)
Change from baseline in proteinuria (g/d) or proteinuria /creatininuria (g/g) at months 3 and 6 then every 6 months
Proportion of patients who used at least one diuretic
Change from baseline in quality of life
Change from baseline in quality of life assessed by PROMIS-29 survey each year

Full Information

First Posted
February 8, 2023
Last Updated
February 8, 2023
Sponsor
University Hospital, Tours
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1. Study Identification

Unique Protocol Identification Number
NCT05732727
Brief Title
Intensification of Blood Pressure Lowering Therapeutics Based on Diuretics Versus Usual Management for Uncontrolled Hypertension IN Patients With Moderate to Severe Chronic Kidney Disease
Acronym
THINK
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 2023 (Anticipated)
Primary Completion Date
March 2027 (Anticipated)
Study Completion Date
March 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Tours

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Disease(CKD), Uncontrolled Hypertension

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Cluster randomized controlled
Masking
None (Open Label)
Masking Description
The very nature of the intervention assessed prevents any form of blinding, neither for care providers, nor for patients. However, the primary outcome is a composite outcome of events which we plan to adjudicate. As a consequence, the primary outcome will be blindly assessed.
Allocation
Randomized
Enrollment
720 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental group
Arm Type
Experimental
Arm Description
Antihypertensive algorithm based on diuretics agents : the clinicians will adjust the drug therapy according to the antihypertensive algorithm based on diuretics agents.
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Standard of care : the clinicians will adapt the antihypertensive strategy according to his own standard of care which can be pharmacological or non-pharmacological therapies.
Intervention Type
Drug
Intervention Name(s)
Antihypertensive algorithm
Intervention Description
Antihypertensive algorithm based on diuretics agents
Intervention Type
Drug
Intervention Name(s)
Standard of care
Intervention Description
standard of care management for antihypertensive therapy intensification
Primary Outcome Measure Information:
Title
End stage kidney disease
Description
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
Title
eGFR decline of at least 40%
Description
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
Title
Cardiovascular events
Description
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
Title
All cause mortality
Description
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
Secondary Outcome Measure Information:
Title
Time to end-stage kidney disease
Description
All components of the composite endpoint will be assessed separately
Time Frame
Up to 36 months
Title
Time to eGFR decrease of at leat 40%
Description
All components of the composite endpoint will be assessed separately
Time Frame
Up to 36 months
Title
Time to the first cardiovascular event among myocardial infarction, heart failure, hospitalization and stroke
Description
All components of the composite endpoint will be assessed separately
Time Frame
Up to 36 months
Title
All-cause mortality
Description
All components of the composite endpoint will be assessed separately
Time Frame
Up to 36 months
Title
Change from baseline in blood pressure
Description
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
Title
Proportion of patients with controlled blood pressure
Description
Proportion of patients with controlled blood pressure at 2 years (PA< 135/85mmHg with home blood pressure monitoring)
Time Frame
24 months
Title
Change from baseline in glomerular filtration rate
Description
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
Title
Change from baseline in proteinuria (g/d) or proteinuria /creatininuria (g/g)
Description
Change from baseline in proteinuria (g/d) or proteinuria /creatininuria (g/g) at months 3 and 6 then every 6 months
Time Frame
From baseline and up to 36 months
Title
Proportion of patients who used at least one diuretic
Time Frame
Up to 36 months
Title
Change from baseline in quality of life
Description
Change from baseline in quality of life assessed by PROMIS-29 survey each year
Time Frame
From baseline and up to 36 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female >=18 years and <80 years of age 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. Uncontrolled office BP (>140 and/or 90 mmHg) confirmed by home blood pressure monitoring (>135/85 mmHg) 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 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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bénédicte Sautenet, MD
Phone
02.34.37.96.86
Ext
+33
Email
benedicte.sautenet@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bénédicte Sautenet, MD
Organizational Affiliation
University Hospital, Tours
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Nephrology, University Hospital of Tours
City
Tours
ZIP/Postal Code
37044
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bénédicte SAUTENET, MD
First Name & Middle Initial & Last Name & Degree
Bénédicte SAUTENET, MD

12. IPD Sharing Statement

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

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