search
Back to results

Effect of Angiotensin Converting Enzyme Inhibitor, Lisinopril, on Renal Blood Flow and Its Correlation With Proteinuria Reduction in Subjects With Type 2 Diabetes and Kidney Disease

Primary Purpose

Type 2 Diabetes

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
ACEI or ARB
Lisinopril
Sponsored by
University of Virginia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 2 Diabetes focused on measuring Diabetic nephropathy

Eligibility Criteria

40 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion For subjects with diabetic nephropathy,

  1. Adults (ages 40 - 75 years)
  2. Diagnosis of type 2 diabetes for more than 5 years
  3. Evidence of diabetic nephropathy as evidenced by

    a. More than 150 mg of proteinuria per day in a 24-hour urine collection, or a spot morning urine protein to creatinine of greater than 0.15, or a spot morning urine albumin to creatinine ratio greater than 100 confirmed on two separate occasions within 12 months

  4. Treatment with a blocker of the renin -angiotensin-aldosterone system (either ACE inhibitor or ARB)

For healthy controls,

  1. Adults (ages 40 - 75 years)
  2. Good general health

Exclusion For subjects with diabetic nephropathy,

  1. Type 1 diabetes
  2. Glomerular filtration rate less than 40 ml/min/1.73 m2 by MDRD formula
  3. Hemoglobin A1C greater than 10%
  4. Blood pressure greater than 150/90 mm Hg or less than 100/55 mm Hg
  5. History of kidney transplantation
  6. Oxygen saturation is less than 80%
  7. History of unstable cardiopulmonary conditions, known intracardiac shunts, or pulmonary hypertension
  8. History of active cancer within the last 3 years

For healthy controls,

  1. History or clinical evidence of any chronic disease
  2. Chronic and regular use of any medications except for oral contraceptives and vitamins
  3. Clinically significant abnormal screening laboratory values
  4. Pregnancy or lactation for women
  5. Blood pressure at screening visit less than 110/60
  6. History of unstable cardiopulmonary conditions, known intracardiac shunts, or pulmonary hypertension
  7. History of active cancer within the last 3 years

Sites / Locations

  • University of Virginia Health System

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Subjects with diabetic nephropathy

Healthy volunteers

Arm Description

Renal blood flow (RBF) will be measured using contrast enhanced ultrasound (CEU) and urine protein will be measured both on and off angiotensin converting enzyme inhibitors (ACEI) or angiotensin receptor blockers (ARB).

Renal blood flow (RBF) will be measured using contrast enhanced ultrasound (CEU) and urine protein will be measured both on and off angiotensin converting enzyme inhibitors (ACEI) or angiotensin receptor blockers (ARB).

Outcomes

Primary Outcome Measures

Change in renal blood flow (RBF)
We will use Contrast Enhanced Ultrasound using Definity as the contrast agent to monitor changes in renal blood flow (RBF).
Change in renal blood flow (RBF)

Secondary Outcome Measures

Change in Proteinuria
Change in Proteinuria

Full Information

First Posted
April 6, 2010
Last Updated
May 10, 2017
Sponsor
University of Virginia
search

1. Study Identification

Unique Protocol Identification Number
NCT01101269
Brief Title
Effect of Angiotensin Converting Enzyme Inhibitor, Lisinopril, on Renal Blood Flow and Its Correlation With Proteinuria Reduction in Subjects With Type 2 Diabetes and Kidney Disease
Official Title
Effect of Angiotensin Converting Enzyme Inhibitor, Lisinopril, on Renal Blood Flow and Its Correlation With Proteinuria Reduction in Subjects With Type 2 Diabetes and Kidney Disease (KXK005).
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Terminated
Why Stopped
Slow Recruitment
Study Start Date
February 2010 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Virginia

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to investigate the effect of a blood pressure medication, Lisinopril, or similar drugs in that class, on the flow of blood to the kidneys. In this study, we will compare blood flow to the kidneys in healthy people that do not have diabetes or kidney disease with people that have diabetes and evidence of kidney disease.
Detailed Description
Blockers of renin angiotensin aldosterone system (RAAS) are considered the standard of care in treatment of diabetic nephropathy. Their effects are thought to be through multiple mechanisms, including reducing intraglomerular pressure. However, due to the lack of a sensitive, practical and noninvasive method of monitoring renal hemodynamics, the magnitude of hemodynamic effects of these agents and its contribution to proteinuria reduction has not been studied in humans. At the same time, it is not clear if treatment with blockers of the RAAS have similar renal hemodynamic effects in individuals with and without diabetes and kidney disease. Up to 36 subjects with type 2 diabetes and more than 150 mg of proteinuria who are on stable doses of ACE inhibitors or angiotensin receptor blockers (ARBs) and up to 18 healthy volunteers will be enrolled in this study. Subjects with type 2 diabetes will be asked to stop their ACE inhibitor or ARB medications for 10 days. Between 7 to 10 days after stopping these medications renal blood flow (RBF) will be measured using contrast enhanced ultrasound (CEU) and urine protein will be measured as well for comparison to baseline. Subjects' ACE inhibitors or ARB will be restarted and RBF measurement using CEU and measurement of urine protein excretion will be repeated after 7 days. For comparison, RBF will be measured by CEU in up to 18 healthy volunteers. They will then be started on Lisinopril 10 mg orally once a day for 7 days. On day 7 RBF measurement will be repeated to assess the effect of ACE inhibitors on RBF in healthy individuals as compared to those with diabetic nephropathy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes
Keywords
Diabetic nephropathy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
6 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Subjects with diabetic nephropathy
Arm Type
Experimental
Arm Description
Renal blood flow (RBF) will be measured using contrast enhanced ultrasound (CEU) and urine protein will be measured both on and off angiotensin converting enzyme inhibitors (ACEI) or angiotensin receptor blockers (ARB).
Arm Title
Healthy volunteers
Arm Type
Active Comparator
Arm Description
Renal blood flow (RBF) will be measured using contrast enhanced ultrasound (CEU) and urine protein will be measured both on and off angiotensin converting enzyme inhibitors (ACEI) or angiotensin receptor blockers (ARB).
Intervention Type
Drug
Intervention Name(s)
ACEI or ARB
Intervention Description
Subjects will be asked to discontinue their usual ACE inhibitor or Angiotensin Receptor Blocker (ARB) for ten days, undergo a CEU using Definity (for renal blood flow assessment) as the contrast agent, then resume their usual ACEI or ARB for ten days, then undergo another CEU using Definity as the contrast agent.
Intervention Type
Drug
Intervention Name(s)
Lisinopril
Intervention Description
Subjects will be undergo a CEU using Definity (for renal blood flow assessment) as the contrast agent, then take Lisinopril 10 mg every day for 7 days, after which they will undergo another CEU using Definity as the contrast agent.
Primary Outcome Measure Information:
Title
Change in renal blood flow (RBF)
Description
We will use Contrast Enhanced Ultrasound using Definity as the contrast agent to monitor changes in renal blood flow (RBF).
Time Frame
Study day 10
Title
Change in renal blood flow (RBF)
Time Frame
Compared to Study Day 17
Secondary Outcome Measure Information:
Title
Change in Proteinuria
Time Frame
Study day 10
Title
Change in Proteinuria
Time Frame
Compared to study day 17

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion For subjects with diabetic nephropathy, Adults (ages 40 - 75 years) Diagnosis of type 2 diabetes for more than 5 years Evidence of diabetic nephropathy as evidenced by a. More than 150 mg of proteinuria per day in a 24-hour urine collection, or a spot morning urine protein to creatinine of greater than 0.15, or a spot morning urine albumin to creatinine ratio greater than 100 confirmed on two separate occasions within 12 months Treatment with a blocker of the renin -angiotensin-aldosterone system (either ACE inhibitor or ARB) For healthy controls, Adults (ages 40 - 75 years) Good general health Exclusion For subjects with diabetic nephropathy, Type 1 diabetes Glomerular filtration rate less than 40 ml/min/1.73 m2 by MDRD formula Hemoglobin A1C greater than 10% Blood pressure greater than 150/90 mm Hg or less than 100/55 mm Hg History of kidney transplantation Oxygen saturation is less than 80% History of unstable cardiopulmonary conditions, known intracardiac shunts, or pulmonary hypertension History of active cancer within the last 3 years For healthy controls, History or clinical evidence of any chronic disease Chronic and regular use of any medications except for oral contraceptives and vitamins Clinically significant abnormal screening laboratory values Pregnancy or lactation for women Blood pressure at screening visit less than 110/60 History of unstable cardiopulmonary conditions, known intracardiac shunts, or pulmonary hypertension History of active cancer within the last 3 years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kambiz Kalantarinia, MD
Organizational Affiliation
University of Virginia
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Virginia Health System
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22908
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Effect of Angiotensin Converting Enzyme Inhibitor, Lisinopril, on Renal Blood Flow and Its Correlation With Proteinuria Reduction in Subjects With Type 2 Diabetes and Kidney Disease

We'll reach out to this number within 24 hrs