Renal Effects of an Angiotensin Converting Enzyme Inhibitor in Adults With Chronic Kidney Disease of Uncertain Aetiology (CKDu)
Primary Purpose
Renal Insufficiency, Chronic
Status
Unknown status
Phase
Phase 1
Locations
Sri Lanka
Study Type
Interventional
Intervention
Enalapril
Calcium Supplement
Sponsored by
About this trial
This is an interventional treatment trial for Renal Insufficiency, Chronic focused on measuring Renal Insufficiency, Chronic, Uncertain aetiology, ACEI
Eligibility Criteria
Inclusion Criteria:
- Males and females between 18-70 years of age
- CKDu Grade 1, 2, 3
- No contraindication for treatment with ACEI
- Informed consent given
Exclusion Criteria:
- Grade 4 CKDu
- Other chronic diseases
- Evidence or suspicion of non renal secondary hypertension
- Diabetes type 1 or 2
- Evidence or suspicion of renovascular disease, obstructive uropathy, or other renal disease
- Treatment with corticosteroids, non-steroidal anti-inflammatory drugs, or immune-suppressive drugs
- Acute myocardial infarction or cerebrovascular accident in the previous 6 months
- Severe uncontrolled hypertension (diastolic blood pressure ≥115 and/or systolic blood pressure ≥220 mm Hg)
- Suspicion or evidence of connective tissue disease, cancer, higher serum aminotransferase concentrations
- Chronic cough; drug or alcohol abuse; pregnancy and breast feeding
- Unwillingness to sign informed consent
Sites / Locations
- General (Teaching) Hospital, Anuradhapura
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Active Comparator
Placebo Comparator
Active Comparator
Placebo Comparator
Arm Label
Enalapril, Proteinuria < 1g/day
Calcium, Proteinuria < 1g/day
Enalapril, Proteinuria > 1g/day
Calcium, Proteinuria > 1g/day
Arm Description
Outcomes
Primary Outcome Measures
Proteinuria
Numerous clinical trials have established that angiotensin-converting enzyme inhibitors (ACEI) are beneficial in slowing progression of renal disease. However the long-term renal effect of these agents in early renal disease is not well demonstrated. In fact the trials which showed benefits with ACEI did show in glomerular disease and evidence is not so strong in tubulo-interstitial disease.
Estimated GFR
In most forms of proteinuric chronic renal disease, glomerular filtration rate continues to decline even when the initial insult has been removed. The cause of CKDu is still unknown. CKDu is a tubulo-interstitial disease with low grade proteinuria. We believe that the place of ACEI for secondary prevention of CKDu progression needs investigation.
Secondary Outcome Measures
All cause mortality
Cardiovascular mortality
Full Information
NCT ID
NCT01624064
First Posted
June 16, 2012
Last Updated
June 19, 2012
Sponsor
Ministry of Health, Sri Lanka
Collaborators
World Health Organization
1. Study Identification
Unique Protocol Identification Number
NCT01624064
Brief Title
Renal Effects of an Angiotensin Converting Enzyme Inhibitor in Adults With Chronic Kidney Disease of Uncertain Aetiology
Acronym
CKDu
Official Title
A Double Blind Clinical Trial to Examine the Renal Effects of an Angiotensin Converting Enzyme Inhibitor (Enalapril) in Adults With Chronic Kidney Disease of Uncertain Aetiology (CKDu)
Study Type
Interventional
2. Study Status
Record Verification Date
June 2012
Overall Recruitment Status
Unknown status
Study Start Date
August 2012 (undefined)
Primary Completion Date
October 2012 (Anticipated)
Study Completion Date
October 2013 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ministry of Health, Sri Lanka
Collaborators
World Health Organization
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Enalapril would significantly reduce progression of renal disease in patients with Chronic Kidney Disease of Uncertain aetiology.
Detailed Description
End Stage Kidney Disease (ESKD) results in reduced life expectancy, quality of life and increased consumption of health care resources. Chronic Kidney Disease of Uncertain aetiology (CKDu) is being increasingly recognized in the North Central Region of Sri Lanka and in certain regions over 25% (unpublished data) of general population is suspected as suffering from CKDu. The number of patients who reach ESKD that requires hemodialysis or transplantation is increasing, highlighting the need to find strategies that slow progression of kidney disease. The need for these strategies is even more critical in Sri Lanka where dialysis in not a preferred treatment option. Treatment strategies should be readily accessible and cheap.
The importance of proteinuria as a significant risk factor for ESKD is well recognized, and treatment that is targeted at reducing proteinuria has been shown to reduce progression of renal disease. The Renin - Angiotensin - Aldosterone - System (RAAS) is directly involved in the regulation of blood pressure, fluid volume, and vascular response to injury and inflammation. The inappropriate activation of this system causes hypertension, fluid retention, and inflammatory, thrombotic, and atherogenic effects that may contribute to end-organ damage in the long term. Angiotensin II mediates hemodynamic effects as well as inflammation and fibrosis in the kidney, heart, and vasculature.
Numerous clinical trials have established that interruption of the RAAS cascade with angiotensin-converting enzyme inhibitors (ACEI) or angiotensin receptor blockers (ARB) is beneficial in slowing progression of renal disease. Reduction of BP lowers proteinuria, but the use of an ACEI or an ARB reduces both proteinuria and the rate of deterioration of renal function beyond those seen with equivalent BP reduction from conventional antihypertensive agents. However, the use of these agents has limitations, with significant numbers of treated patients still demonstrating progressive renal disease. RAAS blockers have been shown to blunt the progression of advanced kidney disease. However the long-term renal effect of these agents in early renal disease is not well demonstrated. In fact the trials which showed benefits with RAAS blockers did show in glomerular disease and evidence is not so strong in tubulo-interstitial disease. The benefits of RAS inhibition seem to depend on the degree of proteinuria at baseline. It is marginal in those with low grade proteinuria.
In most forms of proteinuric chronic renal disease, glomerular filtration rate continues to decline even when the initial insult has been removed. The cause of CKDu is still unknown. CKDu is a tubulo-interstitial disease with low grade proteinuria. We believe that the place of ACEI for secondary prevention of CKDu progression needs investigation
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Insufficiency, Chronic
Keywords
Renal Insufficiency, Chronic, Uncertain aetiology, ACEI
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Enalapril, Proteinuria < 1g/day
Arm Type
Active Comparator
Arm Title
Calcium, Proteinuria < 1g/day
Arm Type
Placebo Comparator
Arm Title
Enalapril, Proteinuria > 1g/day
Arm Type
Active Comparator
Arm Title
Calcium, Proteinuria > 1g/day
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Enalapril
Other Intervention Name(s)
Angiotensin Converting Enzyme Inhibitor
Intervention Description
2.5-20 mg/day
Intervention Type
Drug
Intervention Name(s)
Calcium Supplement
Other Intervention Name(s)
Calcium lactate
Intervention Description
Calcium 2.5-20 mg/day
Primary Outcome Measure Information:
Title
Proteinuria
Description
Numerous clinical trials have established that angiotensin-converting enzyme inhibitors (ACEI) are beneficial in slowing progression of renal disease. However the long-term renal effect of these agents in early renal disease is not well demonstrated. In fact the trials which showed benefits with ACEI did show in glomerular disease and evidence is not so strong in tubulo-interstitial disease.
Time Frame
One year
Title
Estimated GFR
Description
In most forms of proteinuric chronic renal disease, glomerular filtration rate continues to decline even when the initial insult has been removed. The cause of CKDu is still unknown. CKDu is a tubulo-interstitial disease with low grade proteinuria. We believe that the place of ACEI for secondary prevention of CKDu progression needs investigation.
Time Frame
One year
Secondary Outcome Measure Information:
Title
All cause mortality
Time Frame
One year
Title
Cardiovascular mortality
Time Frame
One year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Males and females between 18-70 years of age
CKDu Grade 1, 2, 3
No contraindication for treatment with ACEI
Informed consent given
Exclusion Criteria:
Grade 4 CKDu
Other chronic diseases
Evidence or suspicion of non renal secondary hypertension
Diabetes type 1 or 2
Evidence or suspicion of renovascular disease, obstructive uropathy, or other renal disease
Treatment with corticosteroids, non-steroidal anti-inflammatory drugs, or immune-suppressive drugs
Acute myocardial infarction or cerebrovascular accident in the previous 6 months
Severe uncontrolled hypertension (diastolic blood pressure ≥115 and/or systolic blood pressure ≥220 mm Hg)
Suspicion or evidence of connective tissue disease, cancer, higher serum aminotransferase concentrations
Chronic cough; drug or alcohol abuse; pregnancy and breast feeding
Unwillingness to sign informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Selvarajah Mathu, MBBS, MD
Phone
94-77-7390628
Email
mathuselvarajah@yahoo.com
First Name & Middle Initial & Last Name or Official Title & Degree
Navaratnasingam Janakan, MBBS, MSc, MD
Phone
94-77-7489813
Email
navajanakan@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Selvarajah Mathu, MBBS, MD
Organizational Affiliation
Ministry of Health
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Shanthi Mendis, MBBS, MD
Organizational Affiliation
World Health Organization
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rezvi Sheriff, MBBS, MD
Organizational Affiliation
University of Colombo
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Thilak Abeysekera, MBBS, MD
Organizational Affiliation
Ministry of Health
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Saroj Jayasinghe, MBBS, MD
Organizational Affiliation
University of Colombo
Official's Role
Principal Investigator
Facility Information:
Facility Name
General (Teaching) Hospital, Anuradhapura
City
Anuradhapura
State/Province
North Central
Country
Sri Lanka
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Selvarajah Mathu, MBBS, MD
Phone
94-77-7390628
Email
mathuselvarajah@yahoo.com
First Name & Middle Initial & Last Name & Degree
Selvarajah Mathu, MBBS, MD
12. IPD Sharing Statement
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Renal Effects of an Angiotensin Converting Enzyme Inhibitor in Adults With Chronic Kidney Disease of Uncertain Aetiology
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