Microbiome Dysfunction in Surgical Intensive Care Unit Survivors

Recruiting Observational Study
Sepsis, Trauma Injury
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 110
Sex
Any
Study type
Observational
Participants needed
468 (estimated)
Sponsor
University of Florida · Other
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About This Trial
Oral and gastrointestinal microbiome dysfunction has been demonstrated to be a culprit of various systemic dysfunctions in peripheries such as cardiovascular, nervous, endocrine and musculoskeletal systems. The topic of microbiome dysfunction after surgical intensive care admission is understudied but may be responsible for persistent systemic inflammation clinically observed in surgical intensive…
Trial Locations
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Eligibility Criteria
Sepsis Population Inclusion Criteria 1. Admission to the 46, 77, 87, 4 East, 4 West, or 24-5 ICUs where clinical care can be managed by the critical care organization guided by standard operating procedures. 2. Age ≥18 years 3. Meets Sepsis 3 criteria at time of sepsis diagnosis 4. Has remained in…
Contacts

Ruth Davis, BSN

352-273-8759

ruth.davis@surgery.ufl.edu

CONTACT

Jennifer Lanz, MSN

352-273-5497

jennifer.lanz@surgery.ufl.edu

CONTACT