Phase
Condition
Lung Disease
Treatment
Furosemide (plus potassium chloride)
Placebo (plus placebo electrolyte solution)
Clinical Study ID
Ages 2-10 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
<28 weeks gestation at birth
Post-Menstrual Age (PMA) of 29-32 weeks gestation
Requiring invasive positive pressure respiratory support or NIPPV/NIMV and FiO2 ≥ 25% or requiring non-invasive positive pressure respiratory support (NCPAP≥ 5 cmH20, BiPhasic CPAP) and FiO2 ≥ 30%.
Receiving enteral feedings of 120 mL/kg/day or greater
Expected to be hospitalized for at least 28 days after enrollment
Exclusion
Exclusion Criteria:
Major congenital anomalies (e.g., known renal anomalies, congenital heart disease,congenital diaphragmatic hernia, or chromosomal anomalies)
In infants who had electrolyte testing in the week prior to enrollment, those with aserum creatinine > 1.7 mg/dL, BUN >50 mg/dL, Na <125 mmoL/L, K ≤ 2.5 mmol/L, or Ca ≤ 6 mg/dL. Not having electrolyte testing in the week prior to enrollment is not anexclusion criterion.
Current treatment with Dexamethasone or hydrocortisone for respiratory failure.Treatment with chronic steroids for history of adrenal insufficiency orcardiovascular instability is not an exclusion criterion.
Treatment with any longer-acting diuretic (e.g., chlorothiazide,hydrochlorothiazide, acetazolamide) within 5 days of enrollment where exposure mayresult in carryover effects that confound the N-of-1 trial
Active order for standing, regularly scheduled diuretics (e.g., chronic diuretics)
Non-English speaking
Current treatment with ibuprofen or indocin
Study Design
Connect with a study center
Emory University
Atlanta, Georgia 30303
United StatesActive - Recruiting
RTI International
Durham, North Carolina 27705
United StatesSite Not Available
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio 45229
United StatesActive - Recruiting
Case Western Reserve University, Rainbow Babies and Children's Hospital
Cleveland, Ohio 44106
United StatesActive - Recruiting
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