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N/A N=100 Randomized Double-blind Basic Science

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

Diabetes Type 2

Enrolled (actual)
100
Serious AEs
4.6%
Results posted
Feb 2015
Primary outcome: Primary: Flow Mediated Vasodilation — 4.8; 4.4 percentage change over baseline

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Placebo (Drug); Aliskiren (Drug)
Age
Adult, Older Adult · 21+ yrs
Sex
All
Sponsor
Beth Israel Deaconess Medical Center
Primary completion
Jan 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Flow Mediated Vasodilation
0.3; 0.8; 0.4; 0.9
PRIMARY
Flow Mediated Vasodilation
0.3; 0.8; 0.4; 0.9
PRIMARY
Nitroglycerin Induced Dilation
16.5; 15.2
PRIMARY
Nitroglycerine Induced Vasodilation
0.4; -0.8; -1.4; -0.3
PRIMARY
Skin Blood Flow Before and After Iontophoresis With Acetylcholine and Sodium Nitroprusside
6; -1; -1; 13; -5; 3
PRIMARY
Skin Blood Flow Before and After Iontophoresis With Acetylcholine and Sodium Nitroprusside
6; -1; -1; 13; -5; 3
SECONDARY
Absolute Change in Biochemical Markers of Endothelial Function, sICAM-1, ng/mL
21; 30; 13; 14
SECONDARY
Absolute Change in Biochemical Markers of Endothelial Function, sVCAM-1, ng/mL
335; 236; 185; 106
SECONDARY
Absolute Change in Biochemical Markers of Endothelial Function, t-PAI, pg/mL
45; 30; 54; 26
SECONDARY
Absolute Change in Biochemical Markers of Endothelial Function, C-reactive Protein, μg/mL
-1.0; -0.6; -1.7; -2.0
SECONDARY
Absolute Change in Biochemical Markers of Endothelial Function, E-Selectin, ng/mL
1.9; 0.7; 0.6; -0.7
SECONDARY
Absolute Change in Inflammatory Cytokines and Growth Factors, Osteoprotegerin, pg/mL
-36; 97; -24; 48
SECONDARY
Absolute Change in Inflammatory Cytokines and Growth Factors, Osteopontin, ng/mL
-0.3; 2.2; 1.7; 0.2
SECONDARY
Absolute Change in Inflammatory Cytokines and Growth Factors, G-CSF, pg/mL
1.1; 4.0; 1.9; 4.4
SECONDARY
Absolute Change in Inflammatory Cytokines and Growth Factors, GM-CSF pg/mL
0.4; -0.8; -1.6; 0.4
SECONDARY
Absolute Change in Inflammatory Cytokines and Growth Factors, IL-8, pg/mL
-2.2; -2.0; -2.4; 0.6
SECONDARY
Absolute Change in Inflammatory Cytokines and Growth Factors, MCP-1 pg/mL
-11; -7; 36; 8
SECONDARY
Absolute Change in Inflammatory Cytokines and Growth Factors, MDC ng/mL
-0.09; -0.07; -0.07; 0.04
SECONDARY
Absolute Change in Inflammatory Cytokines and Growth Factors, sCD-40L ng/mL
-0.8; -3.2; 3.3; -3.6
SECONDARY
Absolute Change in Inflammatory Cytokines and Growth Factors, TNFα, pg/mL
-0.15; -0.21; 0.30; -0.09

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.

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 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 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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01165983). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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