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WithdrawnNCT04132648Updated Feb 21, 2023

Curcumin and Exercise in Chronic Kidney Disease

A Phase 2 interventional study of Curcumin and Placebo in Chronic Kidney Diseases, Blood Pressure and Hyperemia, sponsored by University of Iowa. Withdrawn. Open to participants aged 45 Years to 80 Years. Per ClinicalTrials.gov, last updated 2023-02-21.

Sponsored by University of Iowa · Phase 2, Interventional, and Treatment

Why this study was withdrawn
PI left the Institution
Phase
Phase 2
Study type
Interventional
Enrollment
0
Allocation
Randomized
Ages
45 Years to 80 Years
Sex
All
01

Study summary

Chronic kidney disease (CKD) is associated with a pro-oxidative and pro-inflammatory state, and this is thought to contribute to a decrease in vascular function leading to greater cardiovascular disease (CVD) risk. Curcumin supplementation has been shown to reduce oxidative stress and improve endothelial function at rest in healthy older humans, although the magnitude of this effect remains unknown during exercise in CKD. The primary aim of this proposal is to determine whether exercising blood flow and vasoconstrictor responsiveness are improved as a result of acute oral supplementation with curcumin in patients with CKD. We hypothesize that: 1) acute curcumin supplementation will increase steady state exercise blood flow, and 2) reduce vasoconstriction induced by an acute sympathetic stimulus (cold pressor test) CKD.

Read the detailed description

Active muscles require an optimal amount of local blood flow to meet the functional and metabolic demand of the exercising muscle. It is well known that maximal aerobic work capacity and exercise tolerance are reduced in CKD, contributing to functional impairment and loss of independence. A multitude of factors may be responsible for this outcome including reduced blood flow to active muscle beds brought on by greater levels of oxidative stress in CKD. Aging and some individuals with disease (coronary artery disease, hypertension, diabetes) exhibit elevated resting sympathetic nerve activity (SNA), leading to greater vasoconstriction and pressor responses during exercise. However, the magnitude of this effect remains unknown in CKD. Importantly, there are a lack of interventions aimed at improving blood flow and reduce sympathetic mediated vasoconstriction in patients with CKD.

Recent evidence in aging humans suggest that curcumin supplementation improves vascular function by reducing oxidative stress. However, it remains unknown whether acute curcumin supplementation can be regarded as an effective therapeutic strategy aimed at modulating exercise vasodilation and sympathetic mediated vasoconstriction in CKD. Understanding the mechanisms that impair vascular function within exercising muscle is important when understanding implications for systemic blood pressure regulation, cardiovascular disease and functional work capacity in CKD. Therefore, identifying a low cost, non-pharmaceutical intervention and its potential impact on improving vascular function in CKD is a priority in preventative cardiovascular disease medicine.

The present proposal aims to examine the effect of sympathetic vasoconstriction on the differential changes in exercising blood flow in response to acute oral supplementation with curcumin in patients with CKD.

02

Conditions studied

  • Chronic Kidney Diseases
  • Blood Pressure
  • Hyperemia
  • Vasoconstriction

Keywords

  • CKD
  • Exercise
  • Vasoconstrictor Responsiveness
03

In context

Kidney Diseases

3,840 studies on the registry are indexed under Kidney Diseases; 500 are open to participants now.

Browse Kidney Diseases studies →

Lead sponsor

University of Iowa is the lead sponsor of 276 studies on the registry; 35 are open to participants now.

Of its 44 completed or terminated interventional studies of FDA-regulated products, 39 (89%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
45 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria for CKD subjects:

Age 45-80 years old CKD stage III and IV (estimated glomerular filtration rate: 15-60 mL/min/1.73m2) BMI \<40 kg/m2-1 Able to give informed consent

Exclusion Criteria for CKD subjects will include answering yes to the following questions:

  • Active participation in another study?
  • Dialysis?
  • End stage renal disease or kidney failure?
  • Kidney transplant?
  • Sever liver disease or transplant?
  • Diabetes?
  • Angina (i.e., chest discomfort/pain/pressure upon exertion)
  • Severe congestive heart failure?
  • Pacemaker/defibrillator?
  • Heart arrhythmia (i.e. Atrial fibrillation/flutter)?
  • Pregnant, breastfeeding, or unwilling to use adequate birth control?
  • Active infection or antibiotic therapy?
  • Immunosuppressive therapy within the last 3 months?
  • History of stroke?
  • Have you had a heart attack in the last 3 months?
  • Have you taken curcumin in last 3 months?
  • Current use of Hormone Replacement Therapy (if female)?
  • Current smoker?
  • Anemic (Hemoglobin count \<9)?

Inclusion Criteria for healthy middle-age and older subjects:

Age 45-80 years old BMI \<40 kg/m2 1 Able to give informed consent

Exclusion Criteria for health older subjects will include answering yes to the following questions:

  • Chronic kidney disease?
  • Hypertension?
  • Asthma?
  • Heart disease?
  • Clinical depression?
  • Autonomic disorders?
  • Sleep apnea?
  • Sever liver disease or transplant?
  • Diabetes?
  • Heart attack?
  • Angina (i.e., chest discomfort/pain/pressure upon exertion)
  • Severe systolic or congestive heart failure?
  • Heart angioplasty/stent or bypass surgery?
  • Heart valve surgery/replacement or valve disease?
  • Pacemaker/defibrillator?
  • Heart arrhythmia (i.e. Atrial fibrillation/flutter)?
  • Pregnant, breastfeeding, or unwilling to use adequate birth control?
  • Active infection or antibiotic therapy?
  • Immunosuppressive therapy within the last 3 months?
  • Have you taken curcumin in last 3 months?
  • Current use of Hormone Replacement Therapy (if female)?
  • Current smoker?
  • Anemic (Hemoglobin count \<9)?
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Curcumin

    Patients will receive curcumin (Longvida) 2000 mg one time prior to exercise trials

    Drug: Curcumin

  • Placebo comparator
    Placebo

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

    Other: Placebo

Interventions

  • DrugCurcumin

    Oral supplement one time at 2,000 mg

    Also known as: Longvida

  • OtherPlacebo

    Oral supplement one time at 2,000 mg

06

What researchers measure

Primary outcomes

  1. %change forearm vascular condutance (FVC)

    Percentage reduction in FVC in response to acute sympathetic stimulus (cold pressor test; CPT)

    Time frame: 2 hours

Secondary outcomes

  1. forearm blood flow (FBF)

    steady state FBF during forearm hand-grip exercise and CPT

    Time frame: 2 hours

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 21, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04132648
Lead sponsor
University of Iowa
Responsible party
Sponsor
First posted
Oct 21, 2019
Start date
Nov 15, 2020 (estimated)
Primary completion
Nov 1, 2021 (estimated)
Completion
Nov 1, 2021 (estimated)
Last update
Feb 21, 2023

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Feb 2023. You cannot join it, but the record below documents what was studied.

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