Study of the Impact of Fatty Acids From Seal Oil on the Relief of Symptoms Associated With Rheumatoid Arthritis

Status: Recruiting
Location: See location...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This project proposes to conduct the first fully controlled and randomized clinical study demonstrating the impact of DPA-rich sea bass oil on the reduction of symptoms related to rheumatoid arthritis. This unique approach will allow to clinically evaluate the benefits of sea bass oil on the relief of rheumatoid arthritis-related pain in a population suffering from inflammatory arthritis.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Have been diagnosed with RA after the age of 18;

• Have had RA for at least 1 year;

• Meet the 2010 ACR/EULAR criteria;

• Stable disease status for at least 3 months:

‣ Low to moderate activity as measured by the Clinical Disease Activity Index (CDAI);

⁃ Stable dose of DMARD (conventional synthetic Disease Modifying Anti-Rheumatic Drug) for at least 3 months;

⁃ Stable dose of NSAIDs and corticosteroids for at least 1 month;

⁃ Do not take \> 10 mg per day of prednisone.

Locations
Other Locations
Canada
GRMO
RECRUITING
Québec
Contact Information
Primary
Louise Corneau, MSc
louise.corneau@fsaa.ulaval.ca
418-656-2131
Backup
Sonia Pomerleau, MSc
sonia.pomerleau@fsaa.ulaval.ca
418-656-2131
Time Frame
Start Date: 2022-01-20
Estimated Completion Date: 2025-03-31
Participants
Target number of participants: 130
Treatments
Experimental: Seal oil
Daily intake of 15 ml of seal oil containing 534 mg of EPA + 1129 mg of DHA + 530 mg of DPA during 12 weeks
Active_comparator: Control
Daily intake of vegetable oil during 12 weeks
Related Therapeutic Areas
Sponsors
Collaborators: Ministry of Agriculture, Fisheries and Food, Quebec, Groupe De Recherche En Rhumatologie Et Maladies Osseuses Inc.
Leads: Laval University

This content was sourced from clinicaltrials.gov

Similar Clinical Trials