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Respiratory Syncytial Virus (RSV) Follow-Up Study (MK-0476-374)

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Organon

Status

Completed

Conditions

Respiratory Syncytial Virus Bronchiolitis

Study type

Observational

Funder types

Industry

Identifiers

NCT01140048
MK-0476-374 (Other Identifier)
2010_026 (Other Identifier)
0476-374

Details and patient eligibility

About

This is a prospective, multicenter, observational study in participants who completed the 24-week, placebo-controlled MK-0476 Protocol 272 (NCT00076973) study of montelukast in the treatment of respiratory symptoms subsequent to RSV-induced bronchiolitis. The purpose of this study is to better understand the clinical and demographic correlates of asthma and atopic disorders in children (through the age of 6 years) with a history of severe RSV-induced bronchiolitis.

Enrollment

343 patients

Sex

All

Ages

18 months to 6 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • successfully completed MK-0476 Protocol 272
  • had RSV-induced bronchiolitis at entry into Protocol 272

Exclusion criteria

  • had developed or had been diagnosed with any illness or congenital disorder that could be immediately life threatening

Trial design

343 participants in 1 patient group

All Enrolled Participants
Description:
All participants who completed Protocol 272 and were enrolled in Protocol 374

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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