Status:

COMPLETED

Research for Elimination of Lymphatic Filariasis (ICIDR)

Lead Sponsor:

Washington University School of Medicine

Collaborating Sponsors:

National Institute of Allergy and Infectious Diseases (NIAID)

Conditions:

Lymphatic Filariasis

Eligibility:

All Genders

6+ years

Brief Summary

The purpose of this study is to check blood samples for lymphatic filariasis to determine whether the recent Program to Eliminate Lymphatic Filariasis was successful in controlling lymphatic filariasi...

Detailed Description

The purpose of this study is to detect lymphatic filariasis in blood samples to determine whether the recently concluded Program to Eliminate Lymphatic Filariasis has been successful in controlling ly...

Eligibility Criteria

Inclusion

  • Gender, minority and child inclusion: Males and females will be included in population-based village studies without regard to race or ethnic group. There is no reason to exclude pregnant women from population-based studies. There is no reason to exclude children from the village/town studies, and they are included. Younger children will be studied in the school surveys (with large numbers per locality) because they are important sentinels for ongoing filariasis transmission.
  • Eligibility for the cohort study: Subjects in household surveys with positive immunochromotography test, filarial antigen tests, and negative microfilaria thick blood smears and who took diethylcarbamazine and albendazole during the Egyptian Program to Eliminate Lymphatic Filariasis will be invited to participate in the study. Subjects must be residents of localities that have met the Basic Elimination criterion (community microfilaria prevalence by thick smear less than 1% or antigen prevalence rate less than 2%). Consenting subjects will be screened further by testing a sample of venous blood collected after 9 p.m. for microfilaremia by membrane filtration and by performing an ELISA to quantitate filarial antigenemia in serum. Eligible subjects will have no microfilaremia by smear and antigen levels \> 20 ng/ml.

Exclusion

  • Exclusion of children less than 10 years of age from community studies of filarial antigen and microfilaria prevalence is justified because prevalence rates for these parameters are exceedingly low in young children in low transmission areas like Egypt.

Key Trial Info

Start Date :

December 1 2006

Trial Type :

OBSERVATIONAL

End Date :

December 1 2011

Estimated Enrollment :

117500 Patients enrolled

Trial Details

Trial ID

NCT00406627

Start Date

December 1 2006

End Date

December 1 2011

Last Update

September 9 2008

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Ain Shams University

Cairo, Egypt, 11566