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Completed

NCT Number: NCT03597568

Resveratrol and Vascular Function in CKD

The proposed research is clinical study evaluating the therapeutic benefits of resveratrol on vascular function in patients with chronic kidney disease (CKD). The study aims to establish that resveratrol will improve endothelial function and functional performance by reducing oxidative stress and in conjunction with lowering markers of inflammation and oxidative stress.

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Key information

About this study

Patients with chronic kidney disease (CKD) have an exceptionally high risk for cardiovascular disease (CVD), and are 10 times more likely to die from CVD prior to requiring dialysis or kidney transplantation. Inflammation, oxidative stress and vascular dysfunction (impaired endothelial function and increased large elastic artery stiffness), are highly prevalent in CKD and contribute to the high incidence of CVD in this patient population. In addition, patients with CKD suffer from high rates of cognitive decline for which we lack effective therapies. Thus, therapeutic interventions targeting inflammation, oxidative stress, vascular dysfunction in CKD are a priority.

Wine intake, which is known to be rich in various polyphenolic compounds, might have a variety of health benefits. Among these polyphenols, the stilbene derivative resveratrol (RSV), a naturally occurring polyphenol found in grapes and red wine, has recently come to light, as it has been shown to exert potent anti-diabetic, anti-oxidative and anti-inflammatory actions. Importantly, recent studies have demonstrated that resveratrol is well-tolerated (37) and may confer similar benefits in individuals at high risk of CVD, such as improved endothelial function in individuals with metabolic syndrome (i.e. diabetes)

The primary goal of this application is to determine whether 6 wks resveratrol (RSV) supplementation improves vascular function by reducing oxidative stress in a randomized, double-blind, cross-over study of 25 patients with diabetic kidney disease. The investigators hypothesize that: 1) 6 wks RSV will improve vascular function as measured via BA-FMD vs. placebo and 2) that the improvement in vascular function will be related, at least partially, to a reduction in oxidative stress.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • CKD stage III (estimated GFR: 30-60 mL/MIN/1.73m2)
  • Able to give informed consent
  • Angiotensin converting enzyme inhibitor or angiotensin II receptor bloocker for > 3 month prior to the study
  • Type II diabetes mellitus

Exclusion criteria

  • Consuming > 2 glasses/day red wine and/or taking resveratrol or vitamin C supplement in the past 12 months
  • Life expectancy <1 year
  • BMI >40 kg/m2 1
  • Pregnant, breastfeeding, or unwilling to use adequate birth control
  • Uncontrolled hypertension; blood pressure > 140/90
  • Uncontrolled type II DM; AIC > 8.5
  • Currently taking anticoagulants including: coumadin, dalteparin, enoxaparin, haparin, and plavix.
  • Severe liver disease
  • Severe systolic heart failure
  • Hospitalization within the last 3 months
  • Active infection or antibiotic therapy
  • Immunosuppressive therapy within the last year
  • Currently partaking in another research study

Treatment and study plan

Resveratrol

Dietary Supplement

Oral supplementation for 6 weeks

Placebo

Other

Oral supplementation for 6 weeks

Primary outcomes

  1. % Change of Brachial Artery Flow-mediated Dilation

    Time frame: First Baseline measurement to 6 weeks then Second baseline to 6 weeks

    Brachial artery flow-mediated dilation, dilation of the brachial artery in response to shear stress.

    Resveratrol first, then placebo:

    Baseline to 6 weeks on Resveratrol Minimum 2 week washout Baseline to 6 week on placebo

    Placebo first, then resveratrol:

    Baseline to 6 weeks on placebo Minimum washout 2 weeks Baseline to 6 weeks on resveratrol

Secondary outcomes

  1. Change in oxLDL

    Time frame: 6 weeks

    Oxidized low density lipoprotein- (LDL) cholesterol Compare the 6 weeks change from baseline with resveratrol versus placebo

Sponsors and collaborators

Lead sponsor

Diana Jalal

Other

Registry information

Official study title

Effect of 6 Weeks Resveratrol Supplementation on Vascular Function in CKD

Important dates

Study start
2019
Primary completion
2023
Study completion
2023
First posted
Jul 24, 2018
Registry last updated
Nov 1, 2024

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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