Respiratory Events Among Premature Infants

Status Completed

Clinical Trial Summary

Assess the burden of disease associated with RSV infection with premature children in an outpatient setting.

Clinical Trial Description

The primary objective of this prospective study is to assess the burden of disease associated with RSV infection, as measured/determined by rates of outpatient medically attended LRI, emergency room visits and hospitalization among preterm infants (32-≤36 wGA) during RSV season, and its medical/health consequences, as measured by wheezing events, the infant's first RSV season, up to May 2009. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Respiratory Syncytial Virus

Clinical Trial Details

NCT number	NCT00889070
Study type	Observational
Source	MedImmune LLC
Contact
Status	Completed
Phase	N/A
Start date	November 2008
Completion date	May 2009

View Details

See also
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