Curcumin and Vascular and Cognitive Function in Patients With Chronic Kidney Disease
Primary Purpose
Chronic Kidney Diseases, Cognitive Decline
Status
Active
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Curcumin
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Kidney Diseases
Eligibility Criteria
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
Sites / Locations
- University of Iowa
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Curcumin
Placebo
Arm Description
Patients will receive curcumin (Lonvida) 2000 mg PO once a day
Patients will receive placebo pill identical in appearance and taste to the supplement
Outcomes
Primary Outcome Measures
Vascular endothelial function
Brachial artery flow-mediated dilation
Secondary Outcome Measures
Large artery stiffness
Aortic pulse wave velocity
Cognitive function
NIH toolbox battery
Full Information
NCT ID
NCT03223883
First Posted
July 18, 2017
Last Updated
February 20, 2023
Sponsor
Diana Jalal
Collaborators
University of Colorado, Boulder, Stanford University, University of Colorado, Denver
1. Study Identification
Unique Protocol Identification Number
NCT03223883
Brief Title
Curcumin and Vascular and Cognitive Function in Patients With Chronic Kidney Disease
Official Title
Curcumin Supplementation for Improving Vascular and Cognitive Function in Chronic Kidney Disease
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 30, 2018 (Actual)
Primary Completion Date
January 31, 2023 (Actual)
Study Completion Date
August 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Diana Jalal
Collaborators
University of Colorado, Boulder, Stanford University, University of Colorado, Denver
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. 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.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Diseases, Cognitive Decline
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Randomized Double-Blind Placebo-Controlled Clinical Trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Patient, providers, and the investigative team will all be blinded to the randomization.
Allocation
Randomized
Enrollment
88 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Curcumin
Arm Type
Experimental
Arm Description
Patients will receive curcumin (Lonvida) 2000 mg PO once a day
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Patients will receive placebo pill identical in appearance and taste to the supplement
Intervention Type
Drug
Intervention Name(s)
Curcumin
Other Intervention Name(s)
Longvida
Intervention Description
Oral supplement for 12 months
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Oral placebo for 12 months
Primary Outcome Measure Information:
Title
Vascular endothelial function
Description
Brachial artery flow-mediated dilation
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Large artery stiffness
Description
Aortic pulse wave velocity
Time Frame
12 months
Title
Cognitive function
Description
NIH toolbox battery
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
74 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Diana Jalal
Organizational Affiliation
University of Iowa
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Iowa
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Curcumin and Vascular and Cognitive Function in Patients With Chronic Kidney Disease
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