This study aims to evaluate the effectiveness of midodrine as an adjuvant to norepinephrine in weaning critically ill patients from vasopressors
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
112
• Patients in group I will receive midodrine (10 mg orally every 8 hours) in addition to administered concurrently with ongoing intravenous norepinephrine after being on norepinephrine for more than 24 hrs.
Patients in group II with ongoing intravenous norepinephrine only
Sohag University Hospital
Sohag, Egypt
RECRUITINGfollow up of critically ill patients on vasopressors
time of weaning from intravenous vasopressor (norepinephrine)
Time frame: 48 hours
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