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OpenTrials
Completed

NCT Number: NCT01296958

Targeted Screening for Taenia Solium Tapeworms

The purpose of this study is to determine whether screening and treatment of tapeworm carriers can decrease community transmission of Taenia solium parasitic infection.

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Key information

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • All community members are eligible

Exclusion criteria

  • Inability to provide informed consent

Treatment and study plan

Niclosamide

Drug

Single oral dose of niclosamide determined by weight (dose: 11 to 34kg receive 1 gram, 35 to 50kg receive 1.5 grams, over 50kg receive 2 grams)

Community education campaign

Behavioral

Education about prevention of Taenia solium infection provided in a single short (20 minute) interaction with the participant. Education was verbal with visual aids.

Primary outcomes

  1. Porcine seroprevalence

    Time frame: Every 4 months

Secondary outcomes

  1. Intestinal tapeworm prevalence

    Time frame: 16 months

Sponsors and collaborators

Lead sponsor

Oregon Health and Science University

Other

Collaborators

  • National Institute of Neurological Disorders and Stroke (NINDS)
  • National University of San Marcos, Peru

Registry information

Important dates

Study start
2011
Primary completion
2013
Study completion
2013
First posted
Feb 16, 2011
Registry last updated
Oct 24, 2014

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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