N/A
N=100
The Effect of Aliskiren on Endothelial Function in Pre-Diabetes and Diabetes
Diabetes Type 2
Bottom Line
View on ClinicalTrials.gov: NCT01165983 ↗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
| Outcome | Result | p-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
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.