Curcumin and Vascular and Cognitive Function in Patients With Chronic Kidney Disease

Sponsor
Diana Jalal (Other)
Overall Status
Recruiting
CT.gov ID
NCT03223883
Collaborator
University of Colorado, Boulder (Other), Stanford University (Other), University of Colorado, Denver (Other)
88
1
2
67
1.3

Study Details

Study Description

Brief Summary

The proposed research is clinical study evaluating the therapeutic benefits of curcumin on vascular function in patients with chronic kidney disease (CKD). The study aims to establish that curcumin will improve endothelial function and reduce large artery stiffness by reducing oxidative stress and in conjunction with lowering markers of inflammation and oxidative stress. In addition, the study will evaluate the potential benefit of curcumin on cognitive function in patients with CKD.

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

Patients with chronic kidney disease (CKD) are at increased risk of death from cardiovascular disease (CVD). 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, and cognitive impairment in CKD are a biomedical priority.

Curcumin is a natural polyphenol with anti-inflammatory and antioxidant characteristics. It is safe and widely-available. Preliminary data in old mice and healthy middle-aged (MA)/older adult humans indicate that curcumin administration improves endothelial dysfunction and large artery stiffness by reducing oxidative stress and inflammation. Additionally, 12 weeks of curcumin supplementation improves episodic memory in MA/older adults.

The primary goal of this R01 application is to extend previous findings in healthy MA/older adults to patients with CKD, a growing clinical population with extensive baseline vascular dysfunction and cognitive impairment who presently have few treatment options. The hypothesis is that curcumin improves vascular endothelial function and large elastic artery stiffness in MA/older adults with stage IIIb and IV CKD (estimated GFR 15-45 mL/min/1.73m2). The possible mechanisms by which curcumin improves vascular function will be evaluated as well as whether curcumin improves cognitive function in these patients.

Specific aim 1a will determine if 12 months of curcumin supplementation will improve brachial artery-flow mediated dilation (BA-FMD) (endothelial function) and aortic pulse wave velocity (aPWV) (arterial stiffness) compared to placebo (randomized placebo-controlled double-blind study). Specific aim 1b will evaluate whether the curcumin-induced improvements in BA-FMD and aPWV are mediated by reduced oxidative stress, and will evaluate the effects of curcumin on systemic and endothelial cell markers of inflammation and oxidative stress. Importantly, specific aim 2 will evaluate the effects of curcumin supplementation on cognitive function, an important complication of CKD, using the NIH Cognitive Toolbox Battery.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
88 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized Double-Blind Placebo-Controlled Clinical TrialRandomized Double-Blind Placebo-Controlled Clinical Trial
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description:
Patient, providers, and the investigative team will all be blinded to the randomization.
Primary Purpose:
Treatment
Official Title:
Curcumin Supplementation for Improving Vascular and Cognitive Function in Chronic Kidney Disease
Actual Study Start Date :
Jan 30, 2018
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Aug 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Curcumin

Patients will receive curcumin (Lonvida) 2000 mg PO once a day

Drug: Curcumin
Oral supplement for 12 months
Other Names:
  • Longvida
  • Placebo Comparator: Placebo

    Patients will receive placebo pill identical in appearance and taste to the supplement

    Other: Placebo
    Oral placebo for 12 months

    Outcome Measures

    Primary Outcome Measures

    1. Vascular endothelial function [12 months]

      Brachial artery flow-mediated dilation

    Secondary Outcome Measures

    1. Large artery stiffness [12 months]

      Aortic pulse wave velocity

    2. Cognitive function [12 months]

      NIH toolbox battery

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    45 Years to 74 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • CKD stage IIIB and IV

    • BMI<35 kg/m2

    • Able to give informed consent

    Exclusion Criteria:
    • Consuming a diet rich in curcumin or taking curcumin supplements in the past 12 months

    • Life expectancy <1 year

    • Pregnant, breastfeeding, or unwilling to use adequate birth control

    • Uncontrolled hypertension

    • Severe liver disease

    • Severe congestive heart failure

    • Hospitalization within the last 3 months

    • Active infection or antibiotic therapy

    • Immunosuppressive therapy within the last year

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Iowa Iowa City Iowa United States 52242

    Sponsors and Collaborators

    • Diana Jalal
    • University of Colorado, Boulder
    • Stanford University
    • University of Colorado, Denver

    Investigators

    • Principal Investigator: Diana Jalal, University of Iowa

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Diana Jalal, Associate Professor, University of Iowa
    ClinicalTrials.gov Identifier:
    NCT03223883
    Other Study ID Numbers:
    • 201710769
    First Posted:
    Jul 21, 2017
    Last Update Posted:
    Jan 5, 2022
    Last Verified:
    Dec 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 5, 2022