Nitrite-boosting Therapy for Improving Physiological Function in Patients With Chronic Kidney Disease

Running, not enrolling · Phase 4

Conditions studied: Chronic Kidney Disease

In brief

Nitric oxide (NO) is an essential molecule in the body that is decreased in patients with chronic kidney disease (CKD), leading to reductions in vascular, movement ("motor") and cognitive functions. This study will determine if daily oral supplementation (3 months) with a supplement that increases NO in the body, i.e., nitrate-rich beetroot juice, improves vascular, motor and cognitive function in patients with CKD; this study will also provide insight into the biological reasons (mechanisms) by which supplementation with nitrate-rich beetroot juice improves vascular function in these patients. Overall, this research will provide scientific evidence supporting the use of nitrate-rich beetroot juice for preserving physiological function and preventing co-morbid clinical conditions and disability in CKD.

Key facts

Study ID

NCT03826147

Run by

University of Colorado, Boulder

People needed

92

Starts

2019-05-01

Expected to finish

2026-08-01

Last updated by the study team

2026-03-31

Who can join

Age: 30 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• CKD stage II-IV (eGFR using the Modification of Diet in Renal Disease (MDRD) prediction equation 20-90 mL/min/1.73m2; stable renal function in the past 3 months)
• Ability to give informed consent
• Albumin > 3.0 g/dL
• Ability to perform motor and cognitive tests (e.g., can rise from a chair, walk for 6 min, climb 10 stairs)
• Free from alcohol dependence or abuse, as defined by the American Psychiatry Association, Diagnostic and Statistical Manual of Mental Disorders (DSM-V)
• Mini-mental state examination score >21 (rationale: to screen for subjects with major cognitive impairment)
• Blood pressure (BP) >100/60 mmHg for past 3 months (rationale: blood pressure below 100/60 mmHg may elevate the normally small risk of hypotension with nitrate supplementation)
• Not taking medications that will interfere with administered medications (e.g., sildenafil interacts with nitroglycerin)
• Body mass index (BMI) <40 kg/m2 (vascular function measurements can be inaccurate in severely obese patients)

You may not qualify if…

• Life expectancy <1 year
• Uncontrolled hypertension, defined as blood pressure > 160/100 mmHg in the past 3 months
• History of severe liver disease
• History of severe congestive heart failure (i.e., ejection fraction < 35%)
• History of hospitalizations within the last 3 months
• Active infection or antibiotic therapy
• Warfarin use
• Vasculitis requiring immunosuppressive therapy within the last year
• High dietary nitrate intake or current nitrate/nitrite supplementation; hypersensitivity to nitrates or nitrites
• Glucose-6-phosphate dehydrogenase deficiency or blood methemoglobin >2%
• Unwilling to abstain from use of mouthwash or other oral hygiene practices (e.g., tongue scraping) outside of teeth brushing that disrupt the oral microbiome and would interfere with nitrate conversion to nitrite
• Blood donation within 8 weeks prior to enrolling in the study; unwilling to abstain from donating blood for 8 weeks after completing the study

Where it is running

• Integrative Physiology of Aging Laboratory — Boulder, Colorado, United States

Full record on ClinicalTrials.gov

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