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

Curcumin Supplementation for Improving Vascular and Cognitive Function in Chronic Kidney Disease

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03223883
Enrollment
94
Registered
2017-07-21
Start date
2018-06-01
Completion date
2023-01-25
Last updated
2024-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Kidney Diseases, Cognitive Decline

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.

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.

Interventions

DRUGCurcumin

Oral supplement for 12 months

OTHERPlacebo

Oral placebo for 12 months

Sponsors

University of Colorado, Boulder
CollaboratorOTHER
Stanford University
CollaboratorOTHER
University of Colorado, Denver
CollaboratorOTHER
Diana Jalal
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Patient, providers, and the investigative team will all be blinded to the randomization.

Intervention model description

Randomized Double-Blind Placebo-Controlled Clinical Trial

Eligibility

Sex/Gender
ALL
Age
45 Years to 74 Years
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

Design outcomes

Primary

MeasureTime frameDescription
Change in Vascular Endothelial Function at 12 Months12 monthsBrachial artery flow-mediated dilation, changed in diameter in brachial artery in response to shear stress

Secondary

MeasureTime frameDescription
Large Artery Stiffness12 monthsAortic pulse wave velocity
Cognitive Function12 monthsNIH toolbox battery- Executive Function Age-Corrected Standard Score is reported (T-score): This score compares the score of the test-taker to those in the NIH Toolbox nationally representative normative sample at the same age, where a score of 100 indicates performance that was at the national average for the test-taking participant's age. Age-corrected standard scores were derived separately for children (ages 3-17) and adults (ages 18-85). A score of 115 or 85, for example, would indicate that the participant's performance is 1 SD above or below the national average, respectively, when compared with like-aged participants. Higher scores indicate better performance.

Countries

United States

Participant flow

Recruitment details

Study participants were recruited between June 2018 and February 2022 from the Renal Clinics at the University of Iowa Hospital and Clinics (UIHC) and the Iowa City Veterans Affairs Health Care System (VA HCS). All procedures were approved by the University of Iowa and the Iowa City VA HCS Institutional Review Boards and conducted in accordance with the Declaration of Helsinki. All participants provided written documentation of the informed consent process before study participation.

Participants by arm

ArmCount
Curcumin
Patients will receive curcumin (Lonvida) 2000 mg PO once a day Curcumin: Oral supplement for 12 months
45
Placebo
Patients will receive placebo pill identical in appearance and taste to the supplement Placebo: Oral placebo for 12 months
43
Total88

Baseline characteristics

CharacteristicCurcuminPlaceboTotal
Age, Continuous66 years
STANDARD_DEVIATION 8
65 years
STANDARD_DEVIATION 8
66 years
STANDARD_DEVIATION 8
Brachial artery flow-mediated dilation2.8 % change2.6 % change2.7 % change
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants1 Participants1 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
45 Participants42 Participants87 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
4 Participants1 Participants5 Participants
Race (NIH/OMB)
More than one race
0 Participants1 Participants1 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants1 Participants1 Participants
Race (NIH/OMB)
White
41 Participants40 Participants81 Participants
Region of Enrollment
United States
45 participants43 participants88 participants
Sex: Female, Male
Female
10 Participants12 Participants22 Participants
Sex: Female, Male
Male
35 Participants31 Participants66 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
1 / 450 / 43
other
Total, other adverse events
27 / 4521 / 43
serious
Total, serious adverse events
0 / 450 / 43

Outcome results

Primary

Change in Vascular Endothelial Function at 12 Months

Brachial artery flow-mediated dilation, changed in diameter in brachial artery in response to shear stress

Time frame: 12 months

ArmMeasureValue (MEDIAN)
CurcuminChange in Vascular Endothelial Function at 12 Months-0.1 %change
PlaceboChange in Vascular Endothelial Function at 12 Months-0.7 %change
Secondary

Cognitive Function

NIH toolbox battery- Executive Function Age-Corrected Standard Score is reported (T-score): This score compares the score of the test-taker to those in the NIH Toolbox nationally representative normative sample at the same age, where a score of 100 indicates performance that was at the national average for the test-taking participant's age. Age-corrected standard scores were derived separately for children (ages 3-17) and adults (ages 18-85). A score of 115 or 85, for example, would indicate that the participant's performance is 1 SD above or below the national average, respectively, when compared with like-aged participants. Higher scores indicate better performance.

Time frame: 12 months

ArmMeasureValue (MEAN)Dispersion
CurcuminCognitive Function2.62 age-adjusted T-scoreStandard Deviation 9
PlaceboCognitive Function2.25 age-adjusted T-scoreStandard Deviation 9.5
Secondary

Large Artery Stiffness

Aortic pulse wave velocity

Time frame: 12 months

ArmMeasureValue (MEAN)Dispersion
CurcuminLarge Artery Stiffness0.28 m/sStandard Deviation 2.4
PlaceboLarge Artery Stiffness0.36 m/sStandard Deviation 4.2

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026