Cardiovascular Prevention and Rehabilitation Center
Montreal, Quebec, H1T 1N6, Canada
NCT Number: NCT03719794
Subjects with metabolic syndrome are known to possess chronic low-level inflammation. Furthermore, such individuals are at risk of developing atherosclerosis in coronary and other vascular beds. In particular, subjects with metabolic syndrome, prediabetes and type II diabetes mellitus were shown to possess vascular inflammation in carotid atherosclerosis as demonstrated using FDG-PET. In the current pilot proposal, the investigators wish to study the impact of 3-month probiotic supplementation on vascular and systemic inflammation in subjects with metabolic syndrome in the context of a randomized, placebo-controlled, pilot trial.
Looking for future studies?
Notify Me50 year and older
All sexes
Interventional
Not applicable
Montreal, Quebec, H1T 1N6, Canada
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Probiotic supplement once daily (xyz) for 12 weeks
Placebo supplement once daily for 12 weeks
Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.
PET-CT scan of the carotid arteries and ascending thoracic aorta will be performed 2 hours post I.V. The participant will be injected with 18F-FDG.
Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.
Change with hs-CRP
Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.
Change with TNF-α
Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.
Change with MMP-9
Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.
Cognitive functions will be measured at rest with a pen-paper battery test by a neuropsychologist. The investigators will measure change of score to the cognitive tests.
Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.
To evaluate the impact on intestinal microbiota community composition
Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.
Change in fasting glucose
Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.
Change in serum lipids
Montreal Heart Institute
Other
Probiotics for Vascular Inflammation in Metabolic Syndrome (PROMISE): a 12-Week Pilot Study, Randomized,Double-Blinded, Placebo-Controlled Trial
Acronym: PROMISE
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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