Effect of Anti-inflammatory and Anti-microbial Co-supplementations in Traumatic ICU Patients at High Risk of Sepsis (DrNoha-ICU)
Major Trauma, Sepsis
About this trial
This is an interventional prevention trial for Major Trauma
Eligibility Criteria
Inclusion Criteria:
- Adult trauma patients admitted to ICU within 24 hours from trauma onset with injury severity score (ISS) ≥ 16 will be recruited after obtaining informed consent
Exclusion Criteria:
• Patients admitted to ICU after time exceeding 24 hours from trauma onset.
- Patients whose age is less than 18 years.
- Pregnant female.
- Breast feeding women.
- Arrest within 24 hours of admission.
- Immune deficiency or administration of immune suppressant drugs.
- Serum calcium greater than or equal to 10 mg/dl or phosphate greater than or equal 6 mg/dl.
- History of primary parathyroid disease.
- Metabolic bone disease.
- Sarcoidosis.
- End stage renal disease.
- receiving intermittent renal replacement therapy (RRT).
- Failure of enteral feeding or any contraindication to enteral administration.
- Obesity , body mass index (BMI > 35 kg/m2)
- Known contraindication to vitamin C or thiamine (oxalate nephropathy or known glucose-6-phosphate dehydrogenase deficiency)
Sites / Locations
- Mansoura University-Emergency hospital-ICU
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
No Intervention
No Intervention
Active Comparator
Active Comparator
Low risk group
High risk control
High risk DP
High risk CB
no specific treatment will be given
no specific treatment will be given
patients will receive one intramuscular (IM) injection of 400,000 IU of cholecalciferol on day- 1 Also, starting from day 1 and till day 6 (for consequential 6 days), patients will receive lactobacillus probiotics (10 billion colony forming unit) in a dose of 6 sachets per day
Patients will receive vitamin C plus thiamine starting from day 1 in a dose of 1 gm vitamin C and 200 mg thiamine intravenous 4 times at 12-hour intervals for 48 hours