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Can beetroot juice boost brain and body function in kidney patients?
NCT ID NCT03826147
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether drinking nitrate-rich beetroot juice every day for three months can improve blood vessel health, movement, and thinking in people with chronic kidney disease. About 92 participants with moderate kidney disease will receive either the active beetroot juice or a placebo version. The goal is to see if this simple supplement can help prevent disability and other health problems.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- nitrate-rich beetroot juice
- What this could lead to
- If it works, this could point toward a simple dietary supplement to help preserve physical and mental function in chronic kidney disease.
- What could go wrong
- This is a small, early-phase study with only 92 participants, and the benefits may not be large or apply to everyone. Beetroot juice is generally safe but may cause stomach upset or low blood pressure.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
About 92 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
May 2019
- Expected to finish
-
Aug 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
30 to 80 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 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) Exclusion Criteria: * 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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Integrative Physiology of Aging Laboratory
Boulder, Colorado, 80309, United States
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