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OpenTrials
Completed

NCT Number: NCT01133808

Effectiveness of Rotavirus Immunization in Nicaragua

The purpose of the investigators study is to compare the rates of childhood diarrhea at the community level before and after the rotavirus vaccination program in León, Nicaragua. From preliminary studies, the investigators anticipate about a 28% reduction in diarrhea following the vaccination program among children who received the vaccine, and a smaller reduction in diarrhea among children who did not receive the vaccine, due to the effects of "herd immunity". In addition, the investigators will collect stool samples from children who develop diarrhea in order determine the etiology of childhood diarrhea in the post-rotavirus immunization era.

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Key information

Age range

Up to 5 year

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age under 5 years, inclusion in health and demographic surveillance system (CIDS) in Leon, Nicaragua

Exclusion criteria

  • Parents do not consent to child's participation

Sponsors and collaborators

Lead sponsor

Sylvia Becker-Dreps

Other

Collaborators

  • Fogarty International Center of the National Institute of Health
  • Merck Sharp & Dohme LLC
  • Thrasher Research Fund

Registry information

Official study title

Effectiveness of Rotavirus Immunization at the Community Level in Nicaragua

Important dates

Study start
2010
Primary completion
2011
Study completion
2011
First posted
May 31, 2010
Registry last updated
Sep 9, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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