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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03223883
Other study ID # 201710769
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date January 30, 2018
Est. completion date January 25, 2023

Study information

Verified date May 2024
Source University of Iowa
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 88
Est. completion date January 25, 2023
Est. primary completion date January 25, 2023
Accepts healthy volunteers No
Gender All
Age group 45 Years to 74 Years
Eligibility 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

Study Design


Intervention

Drug:
Curcumin
Oral supplement for 12 months
Other:
Placebo
Oral placebo for 12 months

Locations

Country Name City State
United States University of Iowa Iowa City Iowa

Sponsors (4)

Lead Sponsor Collaborator
Diana Jalal Stanford University, University of Colorado, Boulder, University of Colorado, Denver

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Vascular endothelial function Brachial artery flow-mediated dilation 12 months
Secondary Large artery stiffness Aortic pulse wave velocity 12 months
Secondary Cognitive function NIH toolbox battery 12 months
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