- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01296958
Targeted Screening for Taenia Solium Tapeworms
October 22, 2014 updated by: Seth E O'Neal, MD MPH, Oregon Health and Science University
The purpose of this study is to determine whether screening and treatment of tapeworm carriers can decrease community transmission of Taenia solium parasitic infection.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
1811
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Lima, Peru
- San Marcos University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- All community members are eligible
Exclusion Criteria:
- Inability to provide informed consent
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: SCREENING
- Allocation: NON_RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Targeted screening
Screening for intestinal tapeworm carrier followed by treatment with niclosamide as indicated.
|
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)
|
ACTIVE_COMPARATOR: Education
Community education about Taenia solium prevention.
|
Education about prevention of Taenia solium infection provided in a single short (20 minute) interaction with the participant.
Education was verbal with visual aids.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Porcine seroprevalence
Time Frame: Every 4 months
|
Every 4 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Intestinal tapeworm prevalence
Time Frame: 16 months
|
16 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Seth E ONeal, MD MPH, Oregon Health and Science University
- Principal Investigator: Armando Gonzalez, DVM PhD, San Marcos University School of Veterinary Medicine
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2011
Primary Completion (ACTUAL)
January 1, 2013
Study Completion (ACTUAL)
January 1, 2013
Study Registration Dates
First Submitted
February 15, 2011
First Submitted That Met QC Criteria
February 15, 2011
First Posted (ESTIMATE)
February 16, 2011
Study Record Updates
Last Update Posted (ESTIMATE)
October 24, 2014
Last Update Submitted That Met QC Criteria
October 22, 2014
Last Verified
October 1, 2014
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1R21NS069275-01 (NIH)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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