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Omega-3 Supplement

Omega-3 (EPA+DHA) for Coronavirus

Phase 1
Waitlist Available
Led By Arunima Sarkar, MD
Research Sponsored by Hackensack Meridian Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months recruitment efforts (starting on actual study start date)

Summary

This trial is testing if omega-3 supplements can help adults who have ongoing symptoms after recovering from COVID-19. Omega-3s, found in fish oil, might reduce inflammation and improve their condition.

Eligible Conditions
  • Coronavirus

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months recruitment efforts (starting on actual study start date)
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6 months recruitment efforts (starting on actual study start date) for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Feasibility Study for Omega-3 Fatty Acid Supplementation v. Placebo in Adult Patients to Limit Long Covid Syndrome - Compliance as Captured by the Number of Participants Who Remain Compliant for the Whole Duration of the Study by Taking All Pills Daily
Feasibility Study for Omega-3 Fatty Acid Supplementation v. Placebo in Adult Patients to Limit Long Covid Syndrome - Recruitment as Illustrated by the Number of Screen Failures (Potential Participants Approached But Not Interested in Participating).
Feasibility Study for Omega-3 Fatty Acid Supplementation v. Placebo in Adult Patients to Limit Long Covid Syndrome - Retention as Illustrated by the Number of Participants That Initiate But do Not Complete the Study.
Secondary study objectives
Impact of Omega-3 Supplement on Post-covid Symptoms - Cough
Impact of Omega-3 Supplement on Post-covid Symptoms - Fatigue
Impact of Omega-3 Supplement on Post-covid Symptoms - Loss of Smell
+2 more

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Study arm - Omega 3 supplementExperimental Treatment1 Intervention
Omega-3 (EPA+DHA) - Dose is 2,100mg per day via 3 mini-capsules, 2x/day (a total of 6 mini-capsules per day). Each capsule has 252mg of EPA and 102mg of DHA.
Group II: Control arm - placeboPlacebo Group1 Intervention
3 Soybean Oil Placebo capsules 2x/day (a total of 6 mini-capsules per day).

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Logistics

Participation is compensated

You will be compensated for participating in this trial.

Who is running the clinical trial?

Hackensack Meridian HealthLead Sponsor
135 Previous Clinical Trials
30,303 Total Patients Enrolled
Arunima Sarkar, MDPrincipal InvestigatorHackensack Meridian Health
~8 spots leftby Nov 2025