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Relevance of Flavanols for Cardiovascular Function in End-Stage Renal Disease

Phase 2
Withdrawn
Conditions
End Stage Renal Disease
Interventions
Dietary Supplement: low and high dose flavanoids
Registration Number
NCT00835887
Lead Sponsor
RWTH Aachen University
Brief Summary

In this study, the acute and long-term effects of flavanols on vascular function in patients with ESRD will be investigated.

Detailed Description

In order to assess potential acute beneficial effects of flavanols in patients with ESRD, 10 patients undergoing dialysis will be recruited. Subjects will receive a cocoa drink with 16 mg, 250 mg, and 500 mg (in 100 mL water each) flavan-3-ols (40% epicatechine/catechine und 60% procyanidine), respectively, on three consecutively days. The functional/hemodynamic parameters (flowmediated dilation (FMD), venous-occlusion-plethysmography (VOP), blood pressure, heart rate), the biochemical marker of the circulating NO pool (nitrite, nitrate, RNOs), and the plasma levels of flavanols (epicatechine and catechine) will be determined before and after ingestion of the respective cocoadrink.

It is expected that flavanols dose-dependently improve vascular function and that this is associated with an increase in the circulating NO pool.

In order to assess long-term effects of flavanols on vascular function in patients with ESRD.

To characterize potential vascular long-term effects of flavanols in patients with ESRD, a placebo-controlled double-blinded randomized control study will be performed in 40 patients randomized in two groups. Patients will daily receive either a flavanol-poor cocoa drink or a flavanol-rich cocoa drink over a period of three months.

The flavanol-dosis that is necessary to affect vascular function will be assessed as described above. At the beginning of the study, after the first intake of the cocoa (in order to identify nonresponders) and monthly for a period of three months the vascular function will be assessed applying innovative imaging techniques to the brachial artery to assess endothelium-dependent regulation of physicomechanical properties and vascular tone and thus blood flow at the level of the macrocirculation. In parallel new techniques will be applied to assess perfusion at the level of the microcirculation. In particular, measurement of flow-mediated dilation, intima-media-thickness,compliance and stiffness indices will be performed in the macrocirculation of the brachial artery.

Considering the microcirculation, new diagnostic approaches such as Laser-Doppler Flow and peripheral arterial tonometry next to diagnostic approaches such as the venous occlusive plethysmography will be performed. Moreover, the circulating NO pool, markers of inflammation and of oxidative stress, the uremic toxin pcresol and the plasma levels of flavanols will be determined. The exams after month 1, 2, and 3 will be performed in the morning before intake of the cocoa drink. In order to examine potential sustained effects, an additional examination day will take place after 4 month (one month after stopping the flavanol-intake). It is expected that the flavanol-rich cocoa will improve vascular function, which is associated with an increase in the circulating NO-pool and a decrease in inflammatory markers and the marker for oxidative stress.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • patients with end stage renal disease
Exclusion Criteria
  • person under 18 years of age
  • participation in another study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1low and high dose flavanoidsTreatment with low dose flavanoids
2low and high dose flavanoidsTreatment with high dose flavanoids
Primary Outcome Measures
NameTimeMethod
Vascular functionbefore treatment, directly after treatment and 3, resp. 4 months afterwards
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Düsseldorf University Hospital

🇩🇪

Düsseldorf, Germany

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