The primary objective of this study is to describe the safety and tolerance of synagis, compared with placebo, in children below or equal to 2 years of age with Cystic Fibrosis. The secondary objectives of this study relate to both short term and long term outcome variables. They will describe the incidence of RSV hospitalization, total days of RSV hospitalization, use of O2 for RSV, ICU admission for RSV, mechanical ventilation for RSV. To evaluate at 6 months weight gain, changes in use of pulmonary medications from baseline, incidence of pseudomonas bacterial colonization, incidence of documented wheezing episodes, and total days of steroid usage. The hypothesis is that Synagis will be tolerated in patients 2 years of age or below safely.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
2M01RR000036-40
Application #
6412776
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
1974-10-01
Project End
2003-11-30
Budget Start
Budget End
Support Year
40
Fiscal Year
2000
Total Cost
Indirect Cost
Name
Washington University
Department
Type
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
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Obermeit, Lisa C; Beltran, Jessica; Casaletto, Kaitlin B et al. (2017) Evaluating the accuracy of self-report for the diagnosis of HIV-associated neurocognitive disorder (HAND): defining ""symptomatic"" versus ""asymptomatic"" HAND. J Neurovirol 23:67-78

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