We updated the design of this site on December 18, 2017. Learn more.
ClinicalTrials.gov Menu
IMPORTANT: Due to the lapse in government funding, the information on this web site may not be up to date, transactions submitted via the web site may not be processed, and the agency may not be able to respond to inquiries until appropriations are enacted. Updates regarding government operating status and resumption of normal operations can be found at opm.gov.

Incidence of Severe Respiratory Syncytial Virus Infections in Preterm Brazilian Children

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00585481
Recruitment Status : Completed
First Posted : January 3, 2008
Last Update Posted : December 19, 2011
Information provided by (Responsible Party):

December 22, 2007
January 3, 2008
December 19, 2011
January 2008
December 2010   (Final data collection date for primary outcome measure)
To determine the incidence of severe RSV LRTI requiring hospitalization among infants born <35 weeks gestational age for one year. [ Time Frame: 1 Year ]
Not Provided
Complete list of historical versions of study NCT00585481 on ClinicalTrials.gov Archive Site
  • To evaluate the risk and protective factors for severe RSV LRTI in preterm Brazilian infants. [ Time Frame: 1 Year ]
  • To describe the seasonality of RSV infection in three cities in Brazil. [ Time Frame: 1 Year ]
  • To compare the incidence of wheezing episodes by 12 months after maternity hospital discharge among children with and without RSV LRTI. [ Time Frame: 1 Year ]
  • To evaluate the difference in lung function among children with and without RSV LRTI within the first year after maternity hospital discharge. Only children enrolled at one participating site will be evaluated with lung function analysis. [ Time Frame: 1 Year ]
Not Provided
Not Provided
Not Provided
Incidence of Severe Respiratory Syncytial Virus Infections in Preterm Brazilian Children
Incidence of Severe Respiratory Syncytial Virus Infections in Preterm Brazilian Children - BREVI (Brazilian Respiratory Virus in Premature Infants) Study
The primary objective of this study is to determine the incidence of severe RSV LRTI requiring hospitalization among infants born < 35 weeks gestational age for one year of follow-up.
This is an epidemiologic study of the incidence of severe RSV LRTI among Brazilian children born <35WGA. The study will enroll competitively 350 subjects from 3 sites in Brazil. Preterm children will be identified after birth and up to 72 hours after hospital discharge and followed for one year after the enrollment. Subjects will be seen monthly for the first 6 months and bimonthly until one year of follow-up. At each visit, a medical and social history will be updated and a physical examination will be performed. Legal representative will notify study personnel in the event of a respiratory illness or hospital admission at which time the subject will be seen by an investigator. Children with LRTI diagnosed by physical examination will have viral diagnostic tests performed. Subjects with a LRTI not requiring hospitalization will be followed by telephone weekly until illness resolution. Hospitalized children with a LRTI will be followed daily while hospitalized and followed by telephone until illness resolution. All medical interventions and outcomes will be recorded.
Time Perspective: Prospective
Not Provided
Retention:   Samples With DNA
white cells and nasopharyngal aspirate
Non-Probability Sample
Infants < 35 wGA born into or transferred to a participating hospital meeting all of the inclusion criteria and none of the exclusion criteria specified in the protocol will be selected to participate. Subjects will be identified in the NICU or newborn nursery and enrolled in the study 24 hours prior to confirmed hospital discharge or up to 72 hours after maternity hospital discharge date.
  • Respiratory Syncytial Viruses
  • Respiratory Tract Infection
  • Procedure: Samples collection for viral diagnosis

    At Enrollment and Termination Visits all subjects will have phlebotomy performed for RSV antibody levels (3 mL of blood).

    Subjects diagnosed with an LRTI during the study will have a nasopharyngeal lavage (NPL) for viral diagnosis. Phlebotomy for antibody levels will be performed if the current episode represents the first LRTI since study enrollment.

  • Procedure: Lung Function Analysis
    Subjects enrolled in one study site (located in Porto Alegre city) will perform Lung Function Analysis. First measurement will be performed up to Visit 6 and repeated at Termination Visit. Measurements collected in the first analysis will include respiratory compliance and resistance by passive deflation pressure - volume curve, lung volumes by gas dilution method (washout with SF6), lung clearance index with SF6, and maximal flows (rapid thoracic compression from raised volumes).
All subjects will perform samples collection for RSV analysis. Subject's enrolled in Porto Alegre's site will perform lung function tests.
  • Procedure: Samples collection for viral diagnosis
  • Procedure: Lung Function Analysis
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
December 2010
December 2010   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Male and female infants that were born <35 weeks gestational age
  • The inclusion must be done during the following period:

    • 24 hours prior confirmed maternity hospital discharge date, or
    • Up to 72 hours after documented maternity hospital discharge date. In this case, RSV rapid test must be performed and subjects should be enrolled only if the results is negative.
  • Less than 6 months of age at screening
  • Born into or transferred to a participating hospital
  • Able to receive follow-up medical care at the participating site and provide information during the follow-up period
  • The legal representative is capable of understanding and complying with parameters as outlined in the protocol and able and willing to participate in this study, by signing the informed consent approved by an Independent Ethics Committee (IEC)/Institutional Review Board (IRB), after all the aspects of the study that might be relevant for his/her decision to participate are explained and all his/her questions and doubts are elucidated, and prior to the initiation of any screening or study-specific procedures.

Exclusion Criteria:

  • RSV infection prior inclusion.
  • Receipt of palivizumab or other immunoglobulin preparation containing RSV specific antibodies (i.e. RSV hyperimmunoglobulin, polyclonal intravenous immunoglobulin, cytomegalovirus hyperimmunoglobulin, varicella-zoster hyperimmunoglobulin)
Sexes Eligible for Study: All
up to 35 Weeks   (Child)
Contact information is only displayed when the study is recruiting subjects
Not Provided
Not Provided
Statistika Consultoria Ltda
Study Chair: Lino Rodrigues, MD Abbott Laboratórios do Brasil Ltda.
November 2011