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Life sciences · Interventional Study
ClinicalTrials.gov · October 27, 2026
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Interventional Study.
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Registry record from ClinicalTrials.gov (NCT07072871). This is a study registration, not published results. Lead sponsor: PT Royal Medikalink Pharmalab. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 32 participants (ACTUAL). Conditions: Sepsis, Systemic Inflammatory Response Syndrome (SIRS), Critical Illness. Interventions: DIETARY_SUPPLEMENT: Lactiplantibacillus plantarum DAD-13; DRUG: Placebo. Primary outcome measures: Change in Procalcitonin (PCT) levels in ICU sepsis patients after probiotic administration , Day 1 (T0) to Day 4 (T1) of intervention. Brief summary: This study investigated whether giving the probiotic Lactiplantibacillus plantarum DAD-13 to sepsis patients in the intensive care unit (ICU) could help reduce inflammation and improve bowel function. A total of 30 adult ICU patients with sepsis were randomly assigned to receive either the probiotic or a placebo for four days, along with standard treatment. Blood tests were performed to measure inflammatory markers, including procalcitonin (PCT), C-reactive protein (CRP), and interleukin-6 (IL-6), before and after the treatment. The study also observed defecation frequency and stool consistency. Results showed a clinical trend toward lower inflammation levels in the probiotic group and significantly better bowel function. The findings suggest that this probiotic may support immune response and gut health in sepsis patients, although more research is needed to confirm these results.