About this trial
Sepsis is a severe, life-threatening condition caused by an abnormal host response to infection, which includes systemic inflammation, oxidative stress, and increasing organ dysfunction. It is frequently associated with bacterial, viral, fungal, or parasite infections, as well as non-infectious illnesses like trauma and pancreatitis. It remains a primary cause of mortality in hospitals, with rates nearing 40% in severely ill patients. pathophysiological, excessive cytokine release (e.g., TNFα, IL-6, IL-1β) and reactive oxygen/nitrogen species lead to mitochondrial injury, immunosuppression, and multiple organ failure. Sepsis diagnosis is guided byNEWS2 \& a SOFA score ≥2, hypotension, and elevated lactate, while worsening SOFA scores predict poor outcomes. Standard management focusses on early antibiotic therapy, fluid resuscitation, and vasoactive support. Standard anti-inflammatory methods using steroidal or non-steroidal medicines may show little efficacy to improve the patient's clinical outcomes. Adjunctive antioxidant therapies, including vitamins C and E, NAC, and melatonin, have demonstrated reductions in oxidative stress and organ dysfunction. Nicotinamide (NAM) (vitamin B3), a precursor of NAD+/NADP+ critical for energy metabolism and cellular repair, has emerged as a potential therapeutic candidate due to its ability to attenuate cytokine production, modulate immune responses, and mitigate oxidative damage. Usual dose of NAM (500mg-1500mg per day) is generally safe. A dose of 1000 mg was found to be safe and effective in reducing the circulating inflammatory cytokines showing a good profile as an anti-inflammatory adjunct therapy. Higher than usual NAM dose can increase the likelihood of adverse effects, such as diarrhea, increased liver enzymes (rarely occurring at doses exceeding 3 grams per day), symptoms of thrombocytopenia (including increased bruising and bleeding), and stomach upset.
Since the role of NAM as adjunct therapy in sepsis management is not yet established, further large-scale clinical studies are recommended to establish its efficacy and safety in sepsis management.
The aim of our study is to evaluate the efficacy and safety of the addition of Nicotinamide (1000mg oral tablet) as an adjunct therapy to improve the outcome of septic patients.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients older than 18 years of any gender who were admitted to the intensive care unit
Diagnosed as sepsis patient with the Sequential Organ Failure Assessment (SOFA) Score described as an Increase in SOFA score ≥2 points due to infection.
Disqualifiers
Pregnant or lactating women
Patients who had already been taking antioxidant supplements before recruiting.
Patient with contraindications or reported allergies to Nicotinamide.
Trial design
Parallel
Treatments tested in this trial
Nicotinamide 1000 mg
DrugNicotinamide 1000 mg Tablet
Treatment groups
Trial outcomes
Primary outcomes
The Change in SOFA Score
The SOFA (Sequential Organ Failure Assessment) score is a crucial ICU tool that quantifies organ dysfunction with score totaling 0-24, the higher score the worser Outcome
Secondary outcomes
Change in IL-6 levels in serum
serum IL-6 level change will be calculated by subtracting the IL-6 level in Day 7 minus Baseline IL-6 level
Change in NF-kB in serum
serum NF-kB level change will be calculated by subtracting the IL-6 level in Day 7 minus Baseline IL-6 level
Length of ICU stay (days)
Length of ICU stay measured in days from ICU admission until ICU discharge or death, obtained from patient medical records.
28 day Mortality
to determine the mortality rate
Sponsors and contacts
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Ain Shams University
Lead sponsor
Egyptian Chinese University
Collaborator
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