Baking soda and bike rides: a new hope for kidney Patients' fatigue?
NCT ID NCT05928936
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This phase 2 trial tests whether taking sodium bicarbonate pills and doing regular stationary bike exercise can improve exercise capacity in people with chronic kidney disease (CKD). Researchers will enroll 156 adults with CKD, kidney transplant recipients, or healthy controls. Participants will take sodium bicarbonate twice daily and exercise three times a week for 12 weeks. The main goal is to see if these interventions increase the amount of oxygen the body can use during exercise (VO2 peak).
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Sodium bicarbonate (taken as a pill) and supervised exercise training on a stationary bike
- What this could lead to
- If it works, this could point toward a simple, low-cost way to help people with chronic kidney disease feel less tired and be more active.
- What could go wrong
- This is a mid-stage trial with only 156 participants, so results may not apply to everyone. The sodium bicarbonate dose may need frequent adjustment to avoid side effects like metabolic alkalosis.
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
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 156 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2022
- Expected to finish
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Jun 2028
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
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40 to 75 years
- Sex
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Anyone
- Healthy volunteers
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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: * patients with CKD (Stages III and IV), kidney transplant recipients with varying degrees of kidney function, or persons without kidney disease as matched study controls * sedentary and do not regularly exercise (defined as exercising \< 20 minutes twice per week) * CKD patients must have stable renal function (no greater than a decline of estimated glomerular filtration (eGFR) of 1 cc/min/1.73 m2 per month over the prior 6 months) and baseline serum bicarbonate 22-24 mmol/L * comorbid hypertension Exclusion Criteria: * severe CKD (eGFR\<15 cc/min) * metabolic alkalosis * current treatment with bicarbonate * ongoing drug or alcohol abuse * diabetic neuropathy, autonomic dysfunction * any serious disease that might influence survival * anemia with hemoglobin \<10 g/dL * clinical evidence of heart failure * volume overload or ejection fraction below 45% * symptomatic heart disease by EKG, stress test, and/or history * treatment with central α-agonists (clonidine) * myocardial infarction or cerebrovascular accident within the past six months * uncontrolled hypertension (BP\>170/100 mm Hg) * low BP\<100/50 mm Hg * surgery within the past 3 months * pregnancy or plans to become pregnant * inability to exercise on a stationary bicycle * contraindication to temporary withdrawal of α- and β-blockers * peripheral arterial disease * class 3 obesity (BMI\>40) * hypo- or hyperkalemia (K\<3.5meq/L, K\>5.0 meq/L) * current use of immunosuppressive medications (including but not limited to steroids, cyclophosphamide, calcineurin inhibitors, mycophenolate, biologics, methotrexate, etc) * arteriovenous (AV) fistula/graft * any contraindication to MR scanning including cardiac pacemaker, cochlear implants, neurostimulators, implanted devices with metal, any metal in the body that could pose a hazard during scanning, history of claustrophobia
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Atlanta VA Medical Center
RECRUITINGDecatur, Georgia, 30033, United States
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Emory Clinic
RECRUITINGAtlanta, Georgia, 30322, United States
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