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The Effect of Aliskiren on Endothelial Function in Pre-Diabetes and Diabetes

Primary Purpose

Diabetes Type 2

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Placebo
Aliskiren
Sponsored by
Beth Israel Deaconess Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Diabetes Type 2

Eligibility Criteria

21 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Group 1. Subjects At Risk of Developing Type 2 Diabetes

INCLUSION CRITERIA

  1. Ages of 21-80 years
  2. Subjects "at risk" of developing type 2 Diabetes Mellitus (First degree relatives history of type 2 Diabetes Mellitus, History of gestational Diabetes, Known impaired glucose tolerance, Impaired fasting plasma glucose 100-126 mg/dl at the time of enrollment)

EXCLUSION CRITERIA

  1. Treatment with Aliskiren (Tekturna)
  2. Smokers (use of tobacco products in the previous 3 months)
  3. Active or Uncontrolled Cardiovascular Disease

    • Myocardial infarction, or angina within 12 months of study participation
    • Arrhythmia (uncontrolled, highly symptomatic, requiring treatment or life-threatening)
    • CHF (Class III and IV symptoms of heart failure on less than ordinary exertion or at rest)
    • Stroke or Transient Ischemic Attack (TIA) within 12 months of study participation
    • Uncontrolled Hypertension (SBP >180 mmHg or DBP >105 mmHg; 2 abnormal readings during visit)
    • History of previous hypotensive episodes
  4. Liver Disease (AST, ALT, Alk Phos levels > 2x UNL)
  5. Renal Disease (creatinine > 1.7 mg/dL for women and >2.0 mg/dL for men and/or estimated GFR <30 mL/min, history of dialysis, nephrotic syndrome and known renovascular hypertension) at the time of enrollment
  6. Hyperkalemia (serum potassium >5.0 meq/L)
  7. Severe Dyslipidemia (TG > 600 mg/dL or Cholesterol >350 mg/dL)
  8. Any Other Serious Chronic Disease Requiring Active Treatment
  9. Females of Childbearing Potential Not Using an Effective Form of Birth Control as Determined by co-investigators
  10. Pregnancy
  11. Taking Any of the Following Medications:

    • Systemic (not inhaled) Glucocorticoids
    • Antineoplastic Agents
    • Cyclosporine, Ketoconazole, Furosemide, Warfarin
    • Bronchodilators (aminophyline, inhaled beta agonists) on a regular basis
  12. Patient is known to have a history of immunodeficiency diseases, including a positive HIV (ELISA and Western blot) and/or positive Hepatitis B surface antigen (HBsAg) or Hepatitis C test result in the past
  13. History of drug or alcohol abuse within the 12months prior to dosing or evidence of such abuse as indicated by laboratory assays conducted during screening or baseline evaluations

Group 2. Type 2 Diabetic Patients

INCLUSION CRITERIA

  1. Ages of 21-80 years
  2. Type 2 Diabetes Mellitus stable and not expected to change during the study period

EXCLUSION CRITERIA

  1. Treatment with Aliskiren (Tekturna)
  2. Smokers (use of tobacco products in the previous 3 months)
  3. Active or Uncontrolled Cardiovascular Disease

    • Myocardial infarction, or angina within 12 months of study participation
    • Arrhythmia (uncontrolled, highly symptomatic, requiring treatment or life-threatening)
    • CHF (Class III and IV symptoms of heart failure on less than ordinary exertion or at rest)
    • Stroke or Transient Ischemic Attack (TIA) within 12 months of study participation
    • Uncontrolled Hypertension (SBP >180 mmHg or DBP >105 mmHg; 2 abnormal readings during visit)
    • History of previous hypotensive episodes
  4. Liver Disease (AST, ALT, Alk Phos levels > 2x UNL)
  5. Renal Disease (creatinine > 1.7 mg/dL for women and >2.0 mg/dL for men and/or estimated GFR <30 mL/min, history of dialysis, nephrotic syndrome and known renovascular hypertension) at the time of enrollment
  6. Hyperkalemia (serum potassium >5.0 meq/L)
  7. Severe Dyslipidemia (TG > 600 mg/dL or Cholesterol >350 mg/dL)
  8. Any Other Serious Chronic Disease Requiring Active Treatment
  9. Females of Childbearing Potential Not Using an Effective Form of Birth Control as Determined by co-investigators
  10. Pregnancy
  11. Taking Any of the Following Medications:

    • Systemic (not inhaled) Glucocorticoids
    • Antineoplastic Agents
    • Cyclosporine, Ketoconazole, Furosemide, Warfarin
    • Bronchodilators (aminophyline, inhaled beta agonists) on a regular basis
  12. Patient is known to have a history of immunodeficiency diseases, including a positive HIV (ELISA and Western blot) and/or positive Hepatitis B surface antigen (HBsAg) or Hepatitis C test result in the past
  13. History of drug or alcohol abuse within the 12months prior to dosing or evidence of such abuse as indicated by laboratory assays conducted during screening or baseline evaluations
  14. Severe proliferative retinopathy that renders the subject legally blinded
  15. Previous diagnosis of severe gastroparesis diabeticorum due to autonomic neuropathy that has necessitated hospital admission
  16. Presence of non-healing foot ulceration due to severe peripheral diabetic neuropathy
  17. Documented diabetic nephropathy manifested as macro-albuminuria, (2 of 3 urine specimens collected within a 3-6 month period with urine albumin>300 ug/mg creatinine

Sites / Locations

  • Beth Israel Deaconess Medical Center, Joslin Foot Center & Microcirculation Laboratory

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo

Aliskiren

Arm Description

Outcomes

Primary Outcome Measures

Flow Mediated Vasodilation
Using ultrasound, percent change in brachial artery diameter is measured in response to an increase in shear stress from a tightened blood pressure cuff, which causes endothelium-dependent dilatation.
Flow Mediated Vasodilation
Using ultrasound, percent change in brachial artery diameter is measured in response to an increase in shear stress from a tightened blood pressure cuff, which causes endothelium-dependent dilatation.
Nitroglycerin Induced Dilation
Using ultrasound, images are taken pre- and post-vasodilation of the brachial artery induced with a 0.4mg tablet of NTG.
Nitroglycerine Induced Vasodilation
Using ultrasound, images are taken pre- and post-vasodilation of the brachial artery induced with a 0.4mg tablet of NTG.
Skin Blood Flow Before and After Iontophoresis With Acetylcholine and Sodium Nitroprusside
Laser doppler imaging is used to measure microcirculatory changes pre- and post-iontophoresis of acetylcholine and sodium nitroprusside.
Skin Blood Flow Before and After Iontophoresis With Acetylcholine and Sodium Nitroprusside
Laser doppler imaging is used to measure microcirculatory changes pre- and post-iontophoresis of acetylcholine (Ach) and sodium nitroprusside (NaNP).

Secondary Outcome Measures

Absolute Change in Biochemical Markers of Endothelial Function, sICAM-1, ng/mL
Absolute Change in Biochemical Markers of Endothelial Function, sVCAM-1, ng/mL
Absolute Change in Biochemical Markers of Endothelial Function, t-PAI, pg/mL
Absolute Change in Biochemical Markers of Endothelial Function, C-reactive Protein, μg/mL
Absolute Change in Biochemical Markers of Endothelial Function, E-Selectin, ng/mL
Absolute Change in Inflammatory Cytokines and Growth Factors, Osteoprotegerin, pg/mL
Absolute Change in Inflammatory Cytokines and Growth Factors, Osteopontin, ng/mL
Absolute Change in Inflammatory Cytokines and Growth Factors, G-CSF, pg/mL
Absolute Change in Inflammatory Cytokines and Growth Factors, GM-CSF pg/mL
Absolute Change in Inflammatory Cytokines and Growth Factors, IL-8, pg/mL
Absolute Change in Inflammatory Cytokines and Growth Factors, MCP-1 pg/mL
Absolute Change in Inflammatory Cytokines and Growth Factors, MDC ng/mL
Absolute Change in Inflammatory Cytokines and Growth Factors, sCD-40L ng/mL
Absolute Change in Inflammatory Cytokines and Growth Factors, TNFα, pg/mL

Full Information

First Posted
December 15, 2009
Last Updated
February 27, 2017
Sponsor
Beth Israel Deaconess Medical Center
Collaborators
Novartis Pharmaceuticals
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1. Study Identification

Unique Protocol Identification Number
NCT01165983
Brief Title
The Effect of Aliskiren on Endothelial Function in Pre-Diabetes and Diabetes
Official Title
The Effect of Aliskiren on Endothelial Function in Pre-Diabetes and Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
November 2009 (undefined)
Primary Completion Date
January 2012 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beth Israel Deaconess Medical Center
Collaborators
Novartis Pharmaceuticals

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this research is to study and determine the effects of Aliskiren on blood vessels and blood flow. The primary hypothesis is that Aliskiren will increase endothelial function by 30% or more in comparison to the placebo group.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
124 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Title
Aliskiren
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
0mg tablet, taken orally for 12 weeks daily
Intervention Type
Drug
Intervention Name(s)
Aliskiren
Other Intervention Name(s)
Trade name: Tekturna
Intervention Description
150mg tablet, taken orally for 12 weeks daily
Primary Outcome Measure Information:
Title
Flow Mediated Vasodilation
Description
Using ultrasound, percent change in brachial artery diameter is measured in response to an increase in shear stress from a tightened blood pressure cuff, which causes endothelium-dependent dilatation.
Time Frame
Baseline
Title
Flow Mediated Vasodilation
Description
Using ultrasound, percent change in brachial artery diameter is measured in response to an increase in shear stress from a tightened blood pressure cuff, which causes endothelium-dependent dilatation.
Time Frame
12 Weeks post-randomization
Title
Nitroglycerin Induced Dilation
Description
Using ultrasound, images are taken pre- and post-vasodilation of the brachial artery induced with a 0.4mg tablet of NTG.
Time Frame
Baseline
Title
Nitroglycerine Induced Vasodilation
Description
Using ultrasound, images are taken pre- and post-vasodilation of the brachial artery induced with a 0.4mg tablet of NTG.
Time Frame
12 Weeks post-randomization
Title
Skin Blood Flow Before and After Iontophoresis With Acetylcholine and Sodium Nitroprusside
Description
Laser doppler imaging is used to measure microcirculatory changes pre- and post-iontophoresis of acetylcholine and sodium nitroprusside.
Time Frame
Baseline
Title
Skin Blood Flow Before and After Iontophoresis With Acetylcholine and Sodium Nitroprusside
Description
Laser doppler imaging is used to measure microcirculatory changes pre- and post-iontophoresis of acetylcholine (Ach) and sodium nitroprusside (NaNP).
Time Frame
12 Weeks post-randomization
Secondary Outcome Measure Information:
Title
Absolute Change in Biochemical Markers of Endothelial Function, sICAM-1, ng/mL
Time Frame
12 Weeks post-randomization
Title
Absolute Change in Biochemical Markers of Endothelial Function, sVCAM-1, ng/mL
Time Frame
12 Weeks post-randomization
Title
Absolute Change in Biochemical Markers of Endothelial Function, t-PAI, pg/mL
Time Frame
12 Weeks post-randomization
Title
Absolute Change in Biochemical Markers of Endothelial Function, C-reactive Protein, μg/mL
Time Frame
12 Weeks post-randomization
Title
Absolute Change in Biochemical Markers of Endothelial Function, E-Selectin, ng/mL
Time Frame
12 Weeks post-randomization
Title
Absolute Change in Inflammatory Cytokines and Growth Factors, Osteoprotegerin, pg/mL
Time Frame
12 Weeks post-randomization
Title
Absolute Change in Inflammatory Cytokines and Growth Factors, Osteopontin, ng/mL
Time Frame
12 Weeks post-randomization
Title
Absolute Change in Inflammatory Cytokines and Growth Factors, G-CSF, pg/mL
Time Frame
12 Weeks post-randomization
Title
Absolute Change in Inflammatory Cytokines and Growth Factors, GM-CSF pg/mL
Time Frame
12 Weeks post-randomization
Title
Absolute Change in Inflammatory Cytokines and Growth Factors, IL-8, pg/mL
Time Frame
12 Weeks post-randomization
Title
Absolute Change in Inflammatory Cytokines and Growth Factors, MCP-1 pg/mL
Time Frame
12 Weeks post-randomization
Title
Absolute Change in Inflammatory Cytokines and Growth Factors, MDC ng/mL
Time Frame
12 Weeks post-randomization
Title
Absolute Change in Inflammatory Cytokines and Growth Factors, sCD-40L ng/mL
Time Frame
12 Weeks post-randomization
Title
Absolute Change in Inflammatory Cytokines and Growth Factors, TNFα, pg/mL
Time Frame
12 Weeks post-randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Group 1. Subjects At Risk of Developing Type 2 Diabetes INCLUSION CRITERIA Ages of 21-80 years Subjects "at risk" of developing type 2 Diabetes Mellitus (First degree relatives history of type 2 Diabetes Mellitus, History of gestational Diabetes, Known impaired glucose tolerance, Impaired fasting plasma glucose 100-126 mg/dl at the time of enrollment) EXCLUSION CRITERIA Treatment with Aliskiren (Tekturna) Smokers (use of tobacco products in the previous 3 months) Active or Uncontrolled Cardiovascular Disease Myocardial infarction, or angina within 12 months of study participation Arrhythmia (uncontrolled, highly symptomatic, requiring treatment or life-threatening) CHF (Class III and IV symptoms of heart failure on less than ordinary exertion or at rest) Stroke or Transient Ischemic Attack (TIA) within 12 months of study participation Uncontrolled Hypertension (SBP >180 mmHg or DBP >105 mmHg; 2 abnormal readings during visit) History of previous hypotensive episodes Liver Disease (AST, ALT, Alk Phos levels > 2x UNL) Renal Disease (creatinine > 1.7 mg/dL for women and >2.0 mg/dL for men and/or estimated GFR <30 mL/min, history of dialysis, nephrotic syndrome and known renovascular hypertension) at the time of enrollment Hyperkalemia (serum potassium >5.0 meq/L) Severe Dyslipidemia (TG > 600 mg/dL or Cholesterol >350 mg/dL) Any Other Serious Chronic Disease Requiring Active Treatment Females of Childbearing Potential Not Using an Effective Form of Birth Control as Determined by co-investigators Pregnancy Taking Any of the Following Medications: Systemic (not inhaled) Glucocorticoids Antineoplastic Agents Cyclosporine, Ketoconazole, Furosemide, Warfarin Bronchodilators (aminophyline, inhaled beta agonists) on a regular basis Patient is known to have a history of immunodeficiency diseases, including a positive HIV (ELISA and Western blot) and/or positive Hepatitis B surface antigen (HBsAg) or Hepatitis C test result in the past History of drug or alcohol abuse within the 12months prior to dosing or evidence of such abuse as indicated by laboratory assays conducted during screening or baseline evaluations Group 2. Type 2 Diabetic Patients INCLUSION CRITERIA Ages of 21-80 years Type 2 Diabetes Mellitus stable and not expected to change during the study period EXCLUSION CRITERIA Treatment with Aliskiren (Tekturna) Smokers (use of tobacco products in the previous 3 months) Active or Uncontrolled Cardiovascular Disease Myocardial infarction, or angina within 12 months of study participation Arrhythmia (uncontrolled, highly symptomatic, requiring treatment or life-threatening) CHF (Class III and IV symptoms of heart failure on less than ordinary exertion or at rest) Stroke or Transient Ischemic Attack (TIA) within 12 months of study participation Uncontrolled Hypertension (SBP >180 mmHg or DBP >105 mmHg; 2 abnormal readings during visit) History of previous hypotensive episodes Liver Disease (AST, ALT, Alk Phos levels > 2x UNL) Renal Disease (creatinine > 1.7 mg/dL for women and >2.0 mg/dL for men and/or estimated GFR <30 mL/min, history of dialysis, nephrotic syndrome and known renovascular hypertension) at the time of enrollment Hyperkalemia (serum potassium >5.0 meq/L) Severe Dyslipidemia (TG > 600 mg/dL or Cholesterol >350 mg/dL) Any Other Serious Chronic Disease Requiring Active Treatment Females of Childbearing Potential Not Using an Effective Form of Birth Control as Determined by co-investigators Pregnancy Taking Any of the Following Medications: Systemic (not inhaled) Glucocorticoids Antineoplastic Agents Cyclosporine, Ketoconazole, Furosemide, Warfarin Bronchodilators (aminophyline, inhaled beta agonists) on a regular basis Patient is known to have a history of immunodeficiency diseases, including a positive HIV (ELISA and Western blot) and/or positive Hepatitis B surface antigen (HBsAg) or Hepatitis C test result in the past History of drug or alcohol abuse within the 12months prior to dosing or evidence of such abuse as indicated by laboratory assays conducted during screening or baseline evaluations Severe proliferative retinopathy that renders the subject legally blinded Previous diagnosis of severe gastroparesis diabeticorum due to autonomic neuropathy that has necessitated hospital admission Presence of non-healing foot ulceration due to severe peripheral diabetic neuropathy Documented diabetic nephropathy manifested as macro-albuminuria, (2 of 3 urine specimens collected within a 3-6 month period with urine albumin>300 ug/mg creatinine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aristidis Veves, MD
Organizational Affiliation
Beth Israel Deaconess Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beth Israel Deaconess Medical Center, Joslin Foot Center & Microcirculation Laboratory
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
23670354
Citation
Dushay JR, Tecilazich F, Kafanas A, Magargee ML, Auster ME, Gnardellis C, Dinh T, Veves A. Aliskiren improves vascular smooth muscle function in the skin microcirculation of type 2 diabetic patients with normal renal function. J Renin Angiotensin Aldosterone Syst. 2015 Jun;16(2):344-52. doi: 10.1177/1470320313489060. Epub 2013 May 13.
Results Reference
derived

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The Effect of Aliskiren on Endothelial Function in Pre-Diabetes and Diabetes

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