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OpenTrials
Completed

NCT Number: NCT01165983

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

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.

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Key information

Age range

21 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

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

Boston, Massachusetts, 02215, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Placebo

Drug

0mg tablet, taken orally for 12 weeks daily

Aliskiren

Drug

150mg tablet, taken orally for 12 weeks daily

Other names: Trade name: Tekturna

Primary outcomes

  1. Flow Mediated Vasodilation

    Time frame: Baseline

    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.

  2. Flow Mediated Vasodilation

    Time frame: 12 Weeks post-randomization

    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.

  3. Nitroglycerin Induced Dilation

    Time frame: Baseline

    Using ultrasound, images are taken pre- and post-vasodilation of the brachial artery induced with a 0.4mg tablet of NTG.

  4. Nitroglycerine Induced Vasodilation

    Time frame: 12 Weeks post-randomization

    Using ultrasound, images are taken pre- and post-vasodilation of the brachial artery induced with a 0.4mg tablet of NTG.

  5. Skin Blood Flow Before and After Iontophoresis With Acetylcholine and Sodium Nitroprusside

    Time frame: Baseline

    Laser doppler imaging is used to measure microcirculatory changes pre- and post-iontophoresis of acetylcholine and sodium nitroprusside.

  6. Skin Blood Flow Before and After Iontophoresis With Acetylcholine and Sodium Nitroprusside

    Time frame: 12 Weeks post-randomization

    Laser doppler imaging is used to measure microcirculatory changes pre- and post-iontophoresis of acetylcholine (Ach) and sodium nitroprusside (NaNP).

Secondary outcomes

  1. Absolute Change in Biochemical Markers of Endothelial Function, sICAM-1, ng/mL

    Time frame: 12 Weeks post-randomization

  2. Absolute Change in Biochemical Markers of Endothelial Function, sVCAM-1, ng/mL

    Time frame: 12 Weeks post-randomization

  3. Absolute Change in Biochemical Markers of Endothelial Function, t-PAI, pg/mL

    Time frame: 12 Weeks post-randomization

  4. Absolute Change in Biochemical Markers of Endothelial Function, C-reactive Protein, μg/mL

    Time frame: 12 Weeks post-randomization

  5. Absolute Change in Biochemical Markers of Endothelial Function, E-Selectin, ng/mL

    Time frame: 12 Weeks post-randomization

  6. Absolute Change in Inflammatory Cytokines and Growth Factors, Osteoprotegerin, pg/mL

    Time frame: 12 Weeks post-randomization

  7. Absolute Change in Inflammatory Cytokines and Growth Factors, Osteopontin, ng/mL

    Time frame: 12 Weeks post-randomization

  8. Absolute Change in Inflammatory Cytokines and Growth Factors, G-CSF, pg/mL

    Time frame: 12 Weeks post-randomization

  9. Absolute Change in Inflammatory Cytokines and Growth Factors, GM-CSF pg/mL

    Time frame: 12 Weeks post-randomization

  10. Absolute Change in Inflammatory Cytokines and Growth Factors, IL-8, pg/mL

    Time frame: 12 Weeks post-randomization

  11. Absolute Change in Inflammatory Cytokines and Growth Factors, MCP-1 pg/mL

    Time frame: 12 Weeks post-randomization

  12. Absolute Change in Inflammatory Cytokines and Growth Factors, MDC ng/mL

    Time frame: 12 Weeks post-randomization

  13. Absolute Change in Inflammatory Cytokines and Growth Factors, sCD-40L ng/mL

    Time frame: 12 Weeks post-randomization

  14. Absolute Change in Inflammatory Cytokines and Growth Factors, TNFα, pg/mL

    Time frame: 12 Weeks post-randomization

Sponsors and collaborators

Lead sponsor

Beth Israel Deaconess Medical Center

Other

Collaborators

  • Novartis Pharmaceuticals

Registry information

Important dates

Study start
2009
Primary completion
2012
First posted
Jul 20, 2010
Registry last updated
Mar 28, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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