Functional and Lymphocytic Markers of Respiratory Morbidity in Hyperoxic Preemies
Completed
Conditions studied: Prematurity, Symptomatic Respiratory Disease, Bronchopulmonary Dysplasia
In brief
This is an observational study that proposes to collect clinical, physiological, cellular and molecular information in an attempt to identify a set of factors that may predict the risk for persistent lung disease in babies born prematurely.
Key facts
- Study ID
- NCT01607216
- Run by
- University of Rochester
- People needed
- 277
- Starts
- 2011-08-01
- Expected to finish
- 2015-07-01
- Last updated by the study team
- 2020-01-13
Who can join
Age: any, up to 0. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Premature infants born at gestational age 24 0/7 to 35 6/7 week and admitted to the Neonatal Intensive Care Unit or normal newborn nursery at URMC or UB
- Healthy term infants 37 0/7 to 41 6/7 recruited from the birthing centers or Ob/Gyn floors (3-1200 at URMC) prior to discharge
- Infants who are less than or equal to 7 days old
You may not qualify if…
- The infant is not considered to be viable (therapies limited due to futility decision made by clinical care team)
- Congenital heart disease (not including PDA and hemodynamically insignificant VSD or ASD)
- Structural abnormalities of the upper airway, lungs or chest wall
- Other congenital malformations or syndromes that adversely affect life expectancy or cardio-pulmonary development
- Family is unlikely to be available for long-term follow-up as determined by the site investigators dependent on the distance of the infant's residence from the follow-up center and/or family plans to move out of the region
- Family does not speak or understand English
Where it is running
- Women and Children's Hospital of Buffalo — Buffalo, New York, United States
- University of Rochester Medical Center — Rochester, New York, United States
Full record on ClinicalTrials.gov
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