Dexamethasone
DrugIntervention drugs would be administered for 1 or 2 days.
Other names: JEIL Dexamethasone Injection
NCT Number: NCT05136560
The purpose of this study is to investigate the safety and efficacy of early administration of two different doses of dexamethasone in high risk septic patients.
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Notify Me19 year and older
All sexes
Interventional
Phase 1 / Phase 2
Bundang CHA hospital, Seongnam-si, Gyeonggi-do, South Korea
The septic adult patients of high risk would be enrolled in 2 emergency departments.
Sepsis would be defined by Sepsis-3 definition. High risk is defined as initial systolic blood pressure less than 90 mmHg or blood lactate level over 2 mmol/L.
The enrolled patients would be randomized to 3 groups: control, low dose dexamethasone (0.1 mg/kg iv), and high dose dexamethasone (0.2mg/kg iv).
The study drug is blinded and administered after enrollment for 2 days. Sample size would be 102, considering 10% of drop-out rate, allocating 30 patients to each groups.
Efficacy would be evaluated as follows; 28 day and 90 day mortality, time to septic shock, time to shock reversal, administration of steroid according to guideline, ventilator free days, Continuous renal replacement, Length of stay in ICU or hospital, delta SOFA score on day 3 and day 7,
Safety would be evaluated as follows; Superinfection Gastrointestinal bleeding, Hyperglycemia, Hypernatremia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Intervention drugs would be administered for 1 or 2 days.
Other names: JEIL Dexamethasone Injection
Time frame: 28 days
death at 28 day
Time frame: 90 days
death at 90 day
Time frame: up to 1 month, During hospital stay
Time to septic shock after enrollment
Time frame: up to 1 month, During hospital stay
time required for shock reversal
Time frame: up to 1 month, During hospital stay
Need for additional steroid requirement according to the sepsis guideline
Time frame: up to 3 month, During hospital stay
days independent from ventilator care
Time frame: up to 3 month, During hospital stay
requirement of CRRT
Time frame: up to 6 month, During hospital stay
Days spent in intensive care unit (ICU)
Time frame: up to 6 month, During hospital stay
Days spent in hospital
Time frame: 7 days
Change of SOFA score on day 3 and day 7
Time frame: 28 days
secondary infection
Time frame: 14 days
Gastrointestinal bleeding at any amount
Time frame: 7 days
serum glucose >150 mg/dL
Time frame: 7 days
serum sodium >150mmol/L
CHA University
Other
A Randomized, Double-blind, Multi-center Clinical Trial to Evaluate the Safety and Efficacy of Early Administration of Dexamethasone in High-risk Sepsis
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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