Preterm Infant Inhaled Albuterol Dosing

PHASE4CompletedINTERVENTIONAL
Enrollment

14

Participants

Timeline

Start Date

October 24, 2013

Primary Completion Date

December 30, 2014

Study Completion Date

December 30, 2014

Conditions
Bronchopulmonary DysplasiaVery Low Birth Weight
Interventions
DRUG

Varied albuterol dose response

Subjects will be evaluated in 3 sessions. The sessions will occur within a 7 day time span, beginning between 14 or more days from birth and at a corrected gestational age of 28w0d to 33w6d. In each session, pulmonary function tests (PFTs) will be performed prior to and 15 minutes after a dose of albuterol. The dose will be different in each session. In the first session, a sinlge dose of 180 micrograms (2 puffs) of albuterol sulfate via metered dose inhaler. The dose will be 270 micrograms in the second session and 360 micrograms in the third session. PFTs will be performed during quiet sleep while the baby is spontaneously breathing or while the baby is intubated and receiving mechanical ventilation. Resistance and compliance will be measured using the single breath occlusion technique.

Trial Locations (1)

97239

Doernbecher Neonatal Care Center at Oregon Health & Science University, Portland

All Listed Sponsors
lead

Oregon Health and Science University

OTHER

NCT02447250 - Preterm Infant Inhaled Albuterol Dosing | Biotech Hunter | Biotech Hunter