Ireland
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Starting soon Phase 2

Effect of Add-on L-Arginine Therapy on Heart Failure Patients

NCT07394270 · tracked via the Priya Life Science Egypt tracker
Phase
Phase 2
Started
2026-02
Last updated
2026-02-06

Condition(s) studied

Heart Failure

Investigational drug(s) / intervention(s)

L-Arginine PowderPlacebo

L-Arginine Powder: L-arginine 3 gm sachets are used twice daily

Placebo: 2 sachets of placebo are administered per day

Study summary

Heart failure is considered one of the greatest challenges globally. There are various treatment strategies for heart failure. L-Arginine is an amino acid that was found to have beneficial effect on vasculature. This study aims to study the benefits and side effects of using L-arginine on the patients with ejection fraction \<40%

Eligibility

Sex
ALL
Min age
19 Years
Max age
—
Healthy volunteers
No
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

Primary outcome measure(s)

  • Change of Global longitudinal strain value (GLS) of HF patients from the baseline — 6 weeks

Trial sites (1)

FacilityCityRegionStatus
Ain Shams University Cairo Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07394270 on ClinicalTrials.gov ↗ ← All trials in Egypt