Vitamin C, Vitamin B1 and Steroid in Sepsis
Sepsis, Severe
About this trial
This is an interventional treatment trial for Sepsis, Severe
Eligibility Criteria
Inclusion Criteria:
- aged equal or over 20
- admitted to MICU due to severe sepsis or septic shock
Exclusion Criteria:
- Patients who are pregnant
- known history of Vitamin C , Vitamin B or hydrocortisone (or other equivalent products) allergy
Sites / Locations
- Far Eastern Memorial Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
ABC group (Ascorbic acid-Vitamin B1-Hydrocortisone) group
normal saline group
patients in study group, so called" ABC" (Ascorbic acid-Vitamin B1-Hydrocortisone) group, would receive intravenous Thiamine (200mg in 50 mL of 0.9% normal saline and was administered as a 30-min infusion every 12 hours for 4 days or until ICU discharge), Vitamin C (1.5g mixed in a 100-mL solution of normal saline and was administered as an infusion over 30 to 60 min every 6 hours for four days or until ICU discharge) as well as hydrocortisone 50mg every 6 hours (or other equivalent products) for 7 days
patients would receive 50mL 0.9% normal saline, 100 mL 0.9% normal saline with the same infusion rate and hydrocortisone dependent on the discretion of the attending physician