Exploring Approaches With Lower Targets of Blood Pressure and Lipid for Improving Renal Outcome in Advanced Chronic Kidney Disease

Hypertension Clinical Trial

— EXCELSIOR-CKD  

Official title:

Exploring Approaches With Lower Targets of Blood Pressure and Lipid for Improving Renal Outcome in Advanced Chronic Kidney Disease

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06322056
• Other study ID #: 4-2023-1654
• Status: Not yet recruiting
• Phase: N/A
• Start date: May 13, 2024
• Est. completion date: August 31, 2029

Study information

• Verified date: March 2024
• Source: Yonsei University
• Contact: Seung Hyeok Han
• Phone: 82-2-2228-1984
• Email: hansh[@]yuhs.ac
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to prevent kidney disease progression in adults with advanced chronic kidney disease (estimated glomerular filtration rate [eGFR] between 15-45 mL/min/1.73 m2) using intensive blood pressure control and intensive lipid management with 2X2 factorial design.

Description:

The EXploring approaChEs with Lower targets of blood preSsure and lIpid for impOving Renal outcome in advanced Chronic Kidney Disease (EXCELSIOR-CKD) strived to enroll about 642 participants aged ≥19 years with eGFR 15-45 mL/min/1.73 m2, systolic blood pressure (SBP) ≥130 mmHg, and low-density lipoprotein cholesterol (LDL-C) ≥100 mg/dL.

The EXCELSIOR-CKD study is a 2X2 factorial design with factors consisting of: intensive versus standard SBP control (120 vs 140 mmHg), and intensive versus standard LDL-C control (70 vs 100 mg/dL).

The primary hypothesis was that kidney disease progression event rates would be lower in the intensive arms. Participants would be recruited at 13 clinics over approximately a 2-year period, and are planned to be followed for 3 years.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 642
• Est. completion date: August 31, 2029
• Est. primary completion date: May 31, 2029
• Accepts healthy volunteers: No
• Gender: All
• Age group: 19 Years and older

Eligibility

Inclusion Criteria:

• Fulfillment of all of followings

1. At least 19 years old

2. Evidence of CKD defined at least 3 months before and at the time of screening visit with CKD-EPI eGFR =15 to <45 mL/min/1.73 m2

3. SBP of

• 130-180 mmHg on 0 or 1 medication

• 130-170 mmHg on upto 2 medications

• 130-160 mmHg on more than 3 medications

4. LDL-C =100 mg/dL

Exclusion Criteria:

• Any of followings

1. Resistant hypertension or poorly controlled hypertension

• Failure to achieve SBP of <140 mmHg despite using 4 or more antihypertensive medications including diuretics

2. Known secondary cause of hypertension

3. History of renal devervation procedure

4. Glomerulonephritis requiring immunosuppresive agents

5. Autosomal dominant polycystic kidney disease receiving tolvaptan

6. CKD-EPI < 15 mL/min/1.73 m2 or receiving kidney replacement therapy

7. Familial hypercholesterolemia

8. Cardiovascular event or precedure (as defined as myocardial infarction, unstable angina, coronary revascularization, or stroke) within last 3 months or planning to cardiovascular procedure upcoming 3 months at the time of screening visit

9. Symptomatic heart failure within 6 months of left ventricular ejection fraction <45%

10. A medical condition likely to limit survival to less thant 3 years

11. Diagnosis of malignancy within the last 5 years or undergoing chemotherepy or radiotherapy

12. Any organ transplant

13. Advanced cirrhosis (Child-Pugh class B or C) or abnormal liver function test (alanine transaminase or aspartate transaminase =1.5 X upper normal limit)

14. Evidence of active inflammatory muscle disease (polymyositis or dermatomyositis) or creatine kinase elevation (=3 X upper normal limit)

15. History of adverse reaction to HMG-CoA reductase inhibitors or ezetimibe

16. Using any drugs as followings:

• Nicotinic acid

• Macrolide antibiotics

• Systemic imidazole or triazole antifungal agent

• Protease inhibitor

• Nefazodone

• Immunosuppressive agents (glucocorticoid [equivalent to prednisone 10 mg/day over 4 weeks], cyclosporin, mycofenolate, azathioprine, methotrexate, cyclophosphamide, or rituximab)

17. Pregnancy or trying to become pregnant

18. Diabetes mellitus, type I

19. Diabetes mellitus, type II with HbA1c =10.0%

Related Conditions & MeSH terms

• Chronic Kidney Diseases
• Dyslipidemias
• Hypertension
• Kidney Diseases
• Renal Insufficiency, Chronic

Intervention

Drug:
• Intensive control of SBP and intensive control of LDL-C
Eligible participants would be assigned to a SBP target of less than 120 mmHg and a LDL-C target of less than 70 mg/dL.
• Intensive control of SBP and standard control of LDL-C
Eligible participants would be assigned to a SBP target of less than 120 mmHg and a LDL-C target of less than 100 mg/dL.
• Standard control of SBP and intensive control of LDL-C
Eligible participants would be assigned to a SBP target of less than 140 mmHg and a LDL-C target of less than 70 mg/dL.
• Standard control of SBP and standard control of LDL-C
Eligible participants would be assigned to a SBP target of less than 140 mmHg and a LDL-C target of less than 100 mg/dL.

Locations

Country	Name	City	State
Korea, Republic of	Severance Hospital	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Renal composite outcome	Renal composite outcome would be defined as one of followings: A sustained decline in eGFR of 40%,; Initiation of kidney replacement therapy (dialysis or kidney transplantation),; A sustained eGFR <10 mL/min/1.73 m2, or; Death from renal causes	up to 3 years
Secondary	Individual components of renal composite outcome	A sustained decline in eGFR of 40%; Initiation of kidney replacement therapy (dialysis or kidney transplantation),; A sustained eGFR <10 mL/min/1.73 m2; Death from renal causes; Rate of change of eGFR during chronic phase I (12 week to 3 year); Rate of change of eGFR during chronic phase II (24 week to 3 year); Rate of change of eGFR during study period (0 week to 3 year); Cardiovascular composite outcome (defined as one of followings): Death from cardiovascular causes,; Non-fatal myocardial infarction,; Non-fatal stroke (ischemic or hemorrhagic),; Hospitalization for heart failure, or; Revascularization (coronary, carotid, or peripheral artery)	up to 3 years
Secondary	eGFR slopes	A sustained decline in eGFR of 40%; Initiation of kidney replacement therapy (dialysis or kidney transplantation),; A sustained eGFR <10 mL/min/1.73 m2; Death from renal causes; Rate of change of eGFR during chronic phase I (12 week to 3 year); Rate of change of eGFR during chronic phase II (24 week to 3 year); Rate of change of eGFR during study period (0 week to 3 year); Cardiovascular composite outcome (defined as one of followings): Death from cardiovascular causes,; Non-fatal myocardial infarction,; Non-fatal stroke (ischemic or hemorrhagic),; Hospitalization for heart failure, or; Revascularization (coronary, carotid, or peripheral artery)	up to 3 years
Secondary	Cardiovascular composite outcome	A sustained decline in eGFR of 40%; Initiation of kidney replacement therapy (dialysis or kidney transplantation),; A sustained eGFR <10 mL/min/1.73 m2; Death from renal causes; Rate of change of eGFR during chronic phase I (12 week to 3 year); Rate of change of eGFR during chronic phase II (24 week to 3 year); Rate of change of eGFR during study period (0 week to 3 year); Cardiovascular composite outcome (defined as one of followings): Death from cardiovascular causes,; Non-fatal myocardial infarction,; Non-fatal stroke (ischemic or hemorrhagic),; Hospitalization for heart failure, or; Revascularization (coronary, carotid, or peripheral artery)	up to 3 years