Can a common amino acid boost heart function in failure patients?
NCT ID NCT07394270
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This phase 2 trial tests whether adding L-arginine, a natural amino acid, to standard heart failure treatment improves heart function and symptoms. Researchers will enroll 200 stable heart failure patients with low ejection fraction (under 40%). Participants will receive either L-arginine powder or a placebo twice daily for a set period, and the study will measure changes in heart strain, symptoms, and exercise ability.
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 powder
- What this could lead to
- If it works, this could point toward a simple, low-cost supplement to improve heart function and reduce symptoms in heart failure patients.
- What could go wrong
- This is an early phase 2 trial with only 200 participants, so results may not be conclusive. L-arginine may cause side effects or show no benefit over placebo.
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 200 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Feb 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 2027
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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19 years and older
- 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 EF \<40% * eGFR \>30 mL/min/1.73 m2 * Stable patients * Capable and willing to provide written consent Exclusion Criteria: * Patients with implantable cardioverter-defibrillator * Pregnant or lactating fmeales * Patients with a history of sensitivity to L-Arginine or any of the excipients * Acute heart failure patients * Patients use L-arginine supplementation. * Patients with active herpes disease
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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
1 site. 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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Ain Shams University
Cairo, Egypt
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Other studies related to the condition(s) this trial covers.
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- Can AI read heart ultrasounds as well as trained sonographers?