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Arginine Therapy for the Treatment of Pain in Children With Sickle Cell Disease

Arginine for managing pain in kids with Sickle Cell Disease.

Recruiting
7-21 years
All
Phase 1/2

Study Overview: This study investigates if extra arginine can help children with sickle cell disease feel less pain. Sickle cell disease causes painful episodes called vaso-occlusive events (VOE). Arginine is a nutrient found in foods and helps build proteins in the body. People with sickle cell often have low arginine levels, possibly causing more pain.

How It Works: By boosting arginine in the blood, the study aims to decrease pain, reduce the need for pain medications like morphine, and shorten hospital stays. It appears safe and effective for kids with sickle cell during painful episodes, potentially helping them spend less time in pain and in the hospital.

  • Eligibility: For children aged 7-21 with specific types of sickle cell disease (like Hemoglobin SS). Must weigh at least 55 pounds.
  • Exclusions: Children with other types of sickle cell disease, recent hospitalizations, certain health conditions, or medication use may not participate.
  • Potential Benefits: Less pain, fewer pain meds, and reduced hospital stay duration.
Study details
    Sickle Cell Disease

NCT02447874

Emory University

22 August 2026

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