Nerve-Calming amino acid may cut heart risk in kidney disease
NCT ID NCT03982160
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study investigates whether a single infusion of L-arginine, an amino acid, can reduce abnormally high sympathetic nerve activity in people with chronic kidney disease (CKD). High nerve activity is linked to increased cardiovascular risk in CKD patients. Researchers will measure nerve signals in the leg before and after the infusion to see if L-arginine helps lower this activity. The study involves 15 adults aged 35 to 75 with moderate CKD.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- L-Arginine
- What this could lead to
- If successful, this could point toward a new way to lower cardiovascular risk in chronic kidney disease patients by calming an overactive nervous system.
- What could go wrong
- This is a small, early-phase study with only 15 participants, so results may not apply to all patients. The intervention is a single infusion, not a long-term treatment.
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 15 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Feb 2018
- Expected to finish
-
Dec 2026
An estimate. End dates often move.
- Lead sponsor
-
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
-
35 to 75 years
- Sex
-
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 patients classified as Stage 3 and 4 of National Kidney Foundation Classification with estimated glomerular filtration rate (GFR) between 15 and 59 mL/min/1.73 m2 according to the Modification of Diet in Renal Disease (MDRD) formula based on serum creatinine, age, gender, and race. * Men and women 35 to 75 years of age Exclusion Criteria: * myocardial infarction * heart failure * anemia (hemoglobin \<8 g/dl) * cancer with current treatment * previous organ transplantation * immunosuppressant therapy * human immunodeficiency virus infection * pregnancy and/or lactating * current tobacco use * taking menopausal drugs (estradiol) * treatment for diabetic neuropathy * resting heart rate ≥ 100 bpm and * systolic blood pressure ≤ 90 mmHg
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Chronic kidney disease are added.
Genom att skicka in godkänner du våra Användarvillkor
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
-
UT Southwestern
Dallas, Texas, 75390, United States
-
University of Delaware
Newark, Delaware, 19716, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- AI food photos and a chatbot take aim at kidney disease diets
- Can a breathing workout and walks help dialysis patients with irregular heartbeats?
- Can AI-Tailored heat warnings shield chronic disease patients from dangerous temperatures?
- Can a Patient's own kidney cells hold off dialysis?
- A blood test at 50 could flag your risk of five diseases. can an app stop them?
- Two drugs, one goal: can finerenone or semaglutide cut kidney damage markers?