Feasibility of Using the Neovent in Low-Resource Settings

Recruiting N/A Interventional Study
Respiratory Distress of Newborn
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
1 Minute – 28 Days
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
70 (estimated)
Sponsor
Tina Slusher · Other
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About This Trial
Breathing problems are a leading cause of newborn death/sickness worldwide but most of deaths are in low resources areas. Over 99% of newborn death is in countries with limited healthcare resources like Nigeria and Nepal. Background For newborns who have trouble breathing, breathing with a machine that does not require an invasive breathing tube but only small nasal tubes is associated with lower…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Infants ≤ 28 days and \> 30weeks and/or \> 1000 gram (birthweight or admission weight if birthweight unknown) * Mild to moderate respiratory distress (Downes' score 2 - 7) * Parental/guardian permission (informed consent). Exclusion Criteria: * Congenital abnormality such th…
Contacts

Tina M Slusher, MD

612-840-8883

tslusher@umn.edu

CONTACT

Ibukun Sonaike, MBBS, MPH

832-951-0836

Ibukun.Sonaike@hcmed.org

CONTACT