HYDRA is a randomized clinical trial designed to evaluate safety and efficiency of hydrochlorothiazide in critical patients with hypernatremia
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
184
for the experimental group received a hydrochlorothiazide tablet on presentation of 50mg or equivalent enteral solution every 12h (total of 100mg per day) enterally on day 0 (D0) until day 3
for the placebo group will receive one tablet or equivalent volume of enteral solution of inert substance, identical to the hydrochlorothiazide presentations, every 12 hours until day 3
Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo
São Paulo, Brazil
RECRUITINGhypernatremia correction
proportion of patients with hypernatremia correction (serum sodium below 145 mEq / L) at the end of Day 3
Time frame: DAY 3
renal replacement therapy
need to renal replacement therapy
Time frame: 6 months
mechanical ventilation
incidence of mechanical ventilation
Time frame: 6 months
vasoactive drugs
need for vasoactive drugs
Time frame: 6 months
mortality
hospital mortality
Time frame: 6 months
serious adverse events
incidence of serious adverse events 37/5000 incidence of serious adverse events
Time frame: 6 months
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