Beth Israel Deaconess Medical Center, Joslin Foot Center & Microcirculation Laboratory
Boston, Massachusetts, 02215, United States
NCT Number: NCT01165983
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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Notify Me21 year–80 year
All sexes
Interventional
Not applicable
Boston, Massachusetts, 02215, United States
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
Exclusion criteria
Group 2. Type 2 Diabetic Patients
Inclusion criteria
Exclusion criteria
0mg tablet, taken orally for 12 weeks daily
150mg tablet, taken orally for 12 weeks daily
Other names: Trade name: Tekturna
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.
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.
Time frame: Baseline
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
Using ultrasound, images are taken pre- and post-vasodilation of the brachial artery induced with a 0.4mg tablet of NTG.
Time frame: Baseline
Laser doppler imaging is used to measure microcirculatory changes pre- and post-iontophoresis of 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).
Time frame: 12 Weeks post-randomization
Time frame: 12 Weeks post-randomization
Time frame: 12 Weeks post-randomization
Time frame: 12 Weeks post-randomization
Time frame: 12 Weeks post-randomization
Time frame: 12 Weeks post-randomization
Time frame: 12 Weeks post-randomization
Time frame: 12 Weeks post-randomization
Time frame: 12 Weeks post-randomization
Time frame: 12 Weeks post-randomization
Time frame: 12 Weeks post-randomization
Time frame: 12 Weeks post-randomization
Time frame: 12 Weeks post-randomization
Time frame: 12 Weeks post-randomization
Beth Israel Deaconess Medical Center
Other
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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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