Evaluating the Impact of Omega-3 Fatty Acid Supplementation (Soloways™) on Lipid Profiles in Adults With PPARG Polymorphisms

NACompletedINTERVENTIONAL
Enrollment

102

Participants

Timeline

Start Date

February 10, 2022

Primary Completion Date

July 1, 2022

Study Completion Date

November 1, 2022

Conditions
LDL HyperlipoproteinemiaLow-Density-Lipoprotein-Type [LDL] HyperlipoproteinemiaTriglyceride Storage Type I or II Disease
Interventions
DIETARY_SUPPLEMENT

omega-3 fatty acids

The active treatment, supplied by Soloways, LLC., contained omega-3 fatty acids (1000 mg of fish oil, of which 600 mg were eicosapentaenoic acid and 300 mg docosahexaenoic acid) per capsule. The subjects will take 2 capsules daily.

DIETARY_SUPPLEMENT

Placebo

placebo capsules identical in appearance, matched for color coating, shape, and size with omega-3 fatty acids capsule

Trial Locations (1)

630090

Center of New Medical Technologies, Novosibirsk

Sponsors
All Listed Sponsors
collaborator

Center of New Medical Technologies

OTHER

collaborator

Triangel Scientific

INDUSTRY

lead

S.LAB (SOLOWAYS)

OTHER

NCT06154408 - Evaluating the Impact of Omega-3 Fatty Acid Supplementation (Soloways™) on Lipid Profiles in Adults With PPARG Polymorphisms | Biotech Hunter | Biotech Hunter