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Omega-3 Fatty Acids

LOVAZA for Sickle Cell Disease

Phase 2
Waitlist Available
Led By Marie Stuart, M.D.
Research Sponsored by Thomas Jefferson University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights

Study Summary

The purpose of the study is to determine the effectiveness of LOVAZA (fish oil capsules) to decrease inflammation in children and adolescents with Sickle Cell Disease (SCD). It has been found that besides the damage caused by sickle red blood cells themselves, the inflammatory response that occurs in SCD patients could potentially play a significant role in the occurrence of painful episodes or pain crises. The investigators will also study whether the subject/caregiver feels that there is an improvement in the child's quality of life by taking the medication. Besides the effect of LOVAZA on inflammation,the investigators are also testing whether the drug will have a beneficial effect on blood clotting ability (which is known to be increased in SCD) and on the anemia (low red blood cells) that is part of the disease entity.

Eligible Conditions
  • Sickle Cell Disease
  • Beta Thalassemia
  • Inflammation
  • Quality of Life

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
To determine whether supplementation with LOVAZA will exert an anti-inflammatory effect by decreasing levels of the inflammatory biomarker high sensitivity C Reactive Protein (hsCRP) in children and adolescents with Sickle Cell Disease (SCD).
Secondary outcome measures
To determine whether supplementation with LOVAZA will increase health-associated quality of life (QoL) responses as they relate to clinical vasocclusive events (VOC) in children and adolescents with Sickle Cell Disease (SCD).

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: LOVAZAExperimental Treatment1 Intervention
Group II: Placebo capsulePlacebo Group1 Intervention

Find a Location

Who is running the clinical trial?

Thomas Jefferson UniversityLead Sponsor
445 Previous Clinical Trials
145,941 Total Patients Enrolled
Drexel UniversityOTHER
150 Previous Clinical Trials
47,653 Total Patients Enrolled
GlaxoSmithKlineIndustry Sponsor
4,758 Previous Clinical Trials
8,104,082 Total Patients Enrolled

Frequently Asked Questions

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~3 spots leftby May 2025