Cardiovascular Disease Clinical Trial
Official title:
Study of The Effect of Vascular Distensibility on Endothelial-Dependent Vasoreactivity in Subjects With Systolic Hypertension Before and After Receiving Oral Alagebrium or Placebo for 8 Weeks (STRETCH)
The primary objective of the double-blind segment is to compare effects of alagebrium vs placebo on change from baseline in endothelial function, as assessed by flow-mediated vasodilation (FMD).
The secondary objectives of the double-blind segment are to:
- Compare the effects of alagebrium vs placebo on the change from baseline in
endothelial-mediated vasoreactivity immediately after exercise, as assessed by pulse
perfusion-mediated vasodilation (PPMV).
- Confirm results observed in the single-blind segment.
- Explore several variables as potential independent predictors of vascular stiffness and
endothelial function. These parameters include age, body mass index, gender, renal
disease, history of cardiovascular disease, serum cholesterol, and antihypertensive
medication use.
- Provide insight into nitric oxide-dependent endothelial function in the setting of
increased arterial stiffness by determination of substances in the nitric oxide
signaling pathway (specifically, levels of serum cGMP; serum nitrate and nitrite; and
serum asymmetric dimethylarginine [ADMA], an endogenous inhibitor of nitric oxide
synthase).
- Provide insight into the relationship between AGE levels (AGE markers: pentosidine,
furosine), collagen metabolism (collagen markers: procollagen I carboxyterminal
propeptide [PICP], procollagen type I N terminal propeptide [PINP], cross-linked
carboxyterminal telopeptide of Type I collagen [ICTP], n-terminal propeptide of type
III procollagen [PIIINP]), and endothelial function; and insight into the changes in
these markers in response to treatment with an AGE cross-link breaker (alagebrium).
- Provide insight into the relationship between markers of inflammation [specifically,
free and total serum matrix metalloproteinase-1(MMP-1), free tissue inhibitor of
metalloproteinase 1 (TIMP1), intercellular adhesion molecule-1 (ICAM), vascular
cellular adhesion molecule (VCAM), P-selectin, von Willebrand factor (vWf),
interleukin-6 (IL-6), endothelin 1, VEGF, NFkβ, TGF-β, IGF-1 and high-sensitivity C
reactive protein (hs CRP)] and endothelial function; and insight into the changes in
these markers in response to treatment with an AGE cross-link breaker (alagebrium).
;
Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
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