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Recruiting NCT04256330

NCT04256330 Cardiometabolic Health and Inflammatory Resolution

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Clinical Trial Summary
NCT ID NCT04256330
Status Recruiting
Phase
Sponsor Göteborg University
Condition Volunteers
Study Type OBSERVATIONAL
Enrollment 200 participants
Start Date 2020-01-23
Primary Completion 2026-12-31

Trial Parameters

Condition Volunteers
Sponsor Göteborg University
Study Type OBSERVATIONAL
Phase N/A
Enrollment 200
Sex ALL
Min Age 18 Years
Max Age 65 Years
Start Date 2020-01-23
Completion 2026-12-31

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Brief Summary

The aim of this study is to determine how inflammatory resolution impacts cardiometabolic health and disease in subjects that are either lean (18.5-24.9 kg/m2), overweight (25.0-29.9 kg/m2) or obese (\>30.0 kg/m2).

Eligibility Criteria

Inclusion Criteria: * Informed signed consent has been obtained from the volunteer. * The volunteer has a BMI greater than 18.5 kg/m2 Exclusion Criteria: * The study staff contacting a potential participant perceives that the individual has difficulty understanding the information. * An MD determines that the individual is on too many medications to participate * The individual takes a medication that is approved by the MD, but he/she is not willing or not able to wait with any potential morning medication until after their fasted blood-draw. * The individual is younger than 18 years (relevant for the FAINT-1 and FAINT-2 cohorts) * The individual states that they have increased bleeding tendency or are using anti-coagulant (blood thinning) medication. * The individual has some form of chronic inflammation. * The individual regularly uses medication that affects inflammatory resolution (e.g., low-dose aspirin). * The individual uses immunosuppressive drugs (eg, methotrexate). * The indi

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