Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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12 December 2020 |
Main ID: |
NCT03352206 |
Date of registration:
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20/11/2017 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Prevalence Studies After Triple Drug Therapy for Lymphatic Filariasis
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Scientific title:
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Community Studies to Monitor the Impact of Triple Drug Therapy Relative to Double Drug Therapy on Lymphatic Filariasis Infection Indicators |
Date of first enrolment:
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October 18, 2017 |
Target sample size:
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20092 |
Recruitment status: |
Completed |
URL:
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https://clinicaltrials.gov/show/NCT03352206 |
Study type:
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Observational |
Study design:
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Phase:
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Countries of recruitment
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Fiji
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Haiti
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India
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Indonesia
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Papua New Guinea
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Contacts
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Name:
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Gary Weil, MD |
Address:
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Telephone:
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Email:
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Affiliation:
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Washington University School of Medicine |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Age = 5 years (males and females)
- Able to provide informed consent, or parental/guardian consent for young children, and
assent for older children
Exclusion Criteria:
- Unable or unwilling to provide informed consent or (for minors) lacking
parental/guardian consent to participate in the study
Age minimum:
5 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Lymphatic Filariases
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Intervention(s)
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Drug: 2 drug dose - DA
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Drug: 3 drug dose - IDA
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Primary Outcome(s)
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Number of participants with IgG4 antifilarial antibodies in plasma
[Time Frame: One sample collected about 12 months after exposure to treatment]
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Number of participants with microfilaremia as measured with night blood smear testing
[Time Frame: One sample collected about 12 months after exposure to treatment]
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Number of participants with circulating filarial antigenemia (CFA) as measured by the Filaria Test Strip
[Time Frame: One sample collected about 12 months after exposure to treatment]
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Secondary Outcome(s)
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Prevalence of STH (hookworm, ascaris, trichuris and strongyloides) as measured by Kato-katz or PCR
[Time Frame: One comparison about 12 months after exposure to treatment]
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Community prevalence of circulating filarial antigen as measured with filarial test strip
[Time Frame: One comparison about 12 months after exposure to treatment]
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Community prevalence of microfilaremia as measured with night blood smear
[Time Frame: One comparison about 12 months after exposure to treatment]
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Secondary ID(s)
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201710040
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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