Increased Inflammation-resolving Activity by Omega-3 Monoglycerides in Peripheral Blood Mononuclear Cells (PBMC).
PBMC
1 other identifier
observational
200
1 country
1
Brief Summary
The purpose of this biological study is to provide Dr. Samuel Fortin's laboratory with a continuous supply of blood mononuclear cells (PBMCs) so that he can pursue research on the potential beneficial effects of monoglyceride omega-3 fatty acids on the resolution of inflammation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2019
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 12, 2019
CompletedFirst Submitted
Initial submission to the registry
December 15, 2021
CompletedFirst Posted
Study publicly available on registry
December 17, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 1, 2027
April 17, 2026
April 1, 2026
7.8 years
December 15, 2021
April 16, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Number of PBMC cells count
12 months
Interventions
Cells are isolated form the participant's blood donation (4x 10mL k2EDTA tubes per participant) and maintained in culture with LPS, a pro-inflammatory and pro-proliferative agent. Then, PBMC are separated in two, one half treated with MAG-SPM and the other half remains with LPS only. Proliferative activities are measured and compared in both cell dish.
Cells are isolated form the participant's blood donation (4x 10mL k2EDTA tubes per participant) and maintained in culture with LPS, a pro-inflammatory and pro-proliferative agent. Then, PBMC are separated in two, one half treated with MAG-SPM and the other half remains with LPS only. Proliferative activities are measured and compared in both cell dish.
Eligibility Criteria
Healthy adult blood donors
You may qualify if:
- Participant aged of at least 18 years old.
You may not qualify if:
- Participant who use omega-3 supplements and / or anti-inflammatory medication such as, but not limited to - Aspirin, Ibuprofen (Motrin, Advil), Celecoxib (Celebrex), diclofenac (Cambia, Cataflam, Voltaren ) within 7 days of day 1 of the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- SCF Pharmalead
Study Sites (1)
SCF Pharma
Rimouski, Quebec, G0K 1P0, Canada
MeSH Terms
Interventions
Study Officials
- PRINCIPAL INVESTIGATOR
Samuel P Fortin, PhD
SCF Pharma
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- OTHER
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 15, 2021
First Posted
December 17, 2021
Study Start
March 12, 2019
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
January 1, 2027
Last Updated
April 17, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share