ClinicalTrials.gg
CompletedNCT01905436DOLF-LIBERIAUpdated Feb 11, 2022

Mass Drug Administration for Lymphatic Filariasis and Onchocerciasis for Liberia

An observational study in Lymphatic Filariasis, Onchocerciasis and Soil Transmitted Helminth (STH) Infections, sponsored by Washington University School of Medicine. Completed at 1 site in Liberia. Open to participants aged 5 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-02-11.

Sponsored by Washington University School of Medicine · Observational

Study type
Observational
Model
Ecologic or community
Time perspective
Cross-sectional
Enrollment
21,862
Ages
5 Years and older
Sex
All
01

Study summary

Approximately 5,200 people will participate per year. The study population will include females and males over 5 years of age who live in filariasis and onchocerciasis endemic areas. Subject selection will not be based on health status.

Two sites will be studied, and each study will last for 4 years. Participants will be studied only once in cross-sectional surveys. Some subjects may be included in more than one annual population survey, but this is not a longitudinal study.

Investigators will compare annual and semiannual mass drug administration (MDA) for lymphatic filariasis and onchocerciasis, and investigators will compare the impact of these MDA schedules on soil transmitted helminth infections. MDA will be administered by others (Liberian Ministry of Health or Liberian Institute of Biomedical Research).

The investigators will test the hypothesis that semiannual mass drug administration (MDA) is superior to annual MDA for elimination of lymphatic filariasis, onchocerciasis and for control of soil transmitted helminth (STH) infections.

  1. Compare the relative impact and cost effectiveness of annual vs. twice yearly mass drug administration (MDA) for elimination of lymphatic filariasis (LF) in these populations.
  2. Compare the relative impact and cost effectiveness of annual vs. twice yearly mass drug administration (MDA) for elimination of onchocerciasis in these populations.
  3. Study the impact of annual vs. semiannual MDA on soil transmitted helminth (STH) infection in these populations.

Continuation Activities (2019/2020):

Additional one-time cross-sectional surveys will be completed in the Harper site in Maryland district in 2019 and in Lofa in 2020 to measure the long-term impact of MDA on W. bancrofti, O. volvulus, and on STH infection parameters following these cumulative 7-9 rounds of MDA since the baseline survey taken in 2013. Since the last DOLF surveys (3rd follow-ups) in these sites in 2016 \& 2017, respectively, there have been a total of 3 annual rounds of MDA in both areas. These additional surveys will recruit 2,500 participants in the Maryland area villages and 3,200 in the Lofa area villages.

Read the detailed description

Lymphatic filariasis (LF) is a deforming and disabling infectious disease that causes elephantiasis and genital deformity (especially hydroceles). The infection affects some 120 million people in 81 countries in tropical and subtropical regions with well over 1 billion people at risk of acquiring the disease [1]. LF is caused by Wuchereria bancrofti and Brugia spp. (B. malayi and B.timori), nematode parasites that are transmitted by mosquitoes. This study is based on the assumption that currently used MDA regimens and schedules are not optimal for achieving elimination of LF. These regimens (either annual Albendazole (Alb) 400 mg plus diethylcarbamazine 6 mg/kg or Alb 400 mg plus Ivermectin (Iver) 200 µg/kg for LF) were introduced more than 10 years ago.

Onchocerciasis ("Oncho") is similar in some ways to LF in that it is a vector-borne nematode parasitic disease that causes severe disability. In contrast to LF, this disease causes blindness and severe skin disease rather than elephantiasis, and it is spread by black flies instead of mosquitoes. O. volvulus adult worms live in subcutaneous nodules while the adult worms of the LF parasites live in lymphatic vessels. O. volvulus adult worms are larger and less sensitive to available drug treatments than those of the species that cause LF and have a longer lifespan (approximately 14 years rather than the estimated 7 years for LF parasites). More effective drugs or dosing schedules for MDA against Oncho could shorten the number of years needed to interrupt Oncho transmission in areas that previously had high disease rates.

Drugs used for LF MDA are also active against soil transmitted helminth infections (STH, e.g., Ascaris, Hookworm, and Trichuris). De-worming campaigns using anthelmintics usually target special groups of the population, such as schoolchildren, and have limited impact on transmission. Treatment of the total population and semiannual treatments may reduce re-infection considerably and will most likely lead to reduced infection densities and infection prevalence rates. Suppression of STH is an important ancillary benefit of MDA programs for filarial infections. Increasingly control programs for filariasis and STH are being integrated with programs for other parasitic diseases such as schistosomiasis. For this reason, participants will also be tested for schistosomiasis.

Purpose: The study aims to compare the effectiveness once yearly (1X) versus twice yearly (2X) mass drug administration (MDA) for the elimination of lymphatic filariasis, onchocerciasis and for control of soil-transmitted helminth infections (intestinal parasites) in large populations. Mass drug administration will be provided by the Liberian Ministry of Health. This project will assess the impact of the government's public health program.

Procedures: Study procedures include collection of finger prick blood that will be tested for microfilariae by microscopy and for serology testing (antigenemia and antibody testing). Skin snips will be collected and examined by microscopy for the presence of Onchocerca microfilariae. Stool samples will be collected for detection of parasitic worm eggs by microscopy. All assays will be performed in Liberia (filarial serology tests, microfilaria testing, stool examinations).

Washington University researchers developed the protocol, will provide training and guidance to Liberian researchers, and work with them to analyze the data. Liberian researchers will consent the participants, obtain blood, skin and stool specimens, perform laboratory tests on the specimens, and enter data on participants and lab results.

02

Conditions studied

  • Lymphatic Filariasis
  • Onchocerciasis
  • Soil Transmitted Helminth (STH) Infections

Keywords

  • Filariasis
  • Onchocerciasis
  • Albendazole
  • Ivermectin
  • STH Soil Transmitted Helminth infections
  • MDA Mass Drug Administration
03

In context

Elephantiasis, Filarial

42 studies on the registry are indexed under Elephantiasis, Filarial; 5 are open to participants now.

This study's enrollment of 21,862 is above the median of 12,930 across 13 observational studies indexed under Elephantiasis, Filarial.

Browse Elephantiasis, Filarial studies →

Lead sponsor

Washington University School of Medicine is the lead sponsor of 1,803 studies on the registry; 271 are open to participants now.

Of its 329 completed or terminated interventional studies of FDA-regulated products, 216 (66%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
5 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study populations are people who live in areas of Liberia that are co-endemic for lymphatic filariasis and onchocerciasis.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

    • Study areas should be endemic for filariasis and onchocerciasis.
    • Study population have limited or no prior experience with MDA. Males and Females greater than 5 years of age.

Exclusion criteria

Exclusion Criteria:

    • Children less than 5 years of age.
    • Children who weigh less than 15 kg (33 lb)
05

Study design

Observational model
Ecologic or community
Time perspective
Cross-sectional
Enrollment
21,862 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Annual Mass Drug Administration

    This group will receive annual mass drug administration (Albendazole 400 mg plus Ivermectin) provided by the Liberian Ministry of Health.

    Drug: Annual versus Semiannual Albendazole plus Ivermectin Mass Drug Administration

  • Semiannual Mass Drug Administration

    This group will receive semi-annual mass drug administration (Albendazole 400 mg plus Ivermectin) provided by the Liberian Ministry of Health.

    Drug: Annual versus Semiannual Albendazole plus Ivermectin Mass Drug Administration

Interventions

  • DrugAnnual versus Semiannual Albendazole plus Ivermectin Mass Drug Administration

    Annual or semiannual Albendazole plus Ivermectin, administered by the Liberian Ministry of Health.

    Also known as: Albenza (Albendazole); Ivermectin, also known as Mectizan or Stromectol.

06

What researchers measure

Primary outcomes

  1. Prevalence of W. bancrofti microfilaria (4 years)

    Prevalence of W. bancrofti microfilaria (mf) is a binary outcome measured by the presence/absence of W. bancrofti mf in three-line thick smears prepared with a measured 60 microliter quantity of finger prick blood collected between 8pm-2am. The species of mf will be determined by morphological criteria.

    Time frame: 4 years

  2. Prevalence of W. bancrofti filarial antigenemia (4 years)

    Prevalence of this outcome measure is determined by the percentage (%) of individuals with positive tests for the W. bancrofti filarial antigen. Blood will be tested for filarial antigenemia using the Alere Filariasis Test Strip (FTS).

    Time frame: 4 years

Secondary outcomes

  1. Prevalence of O. volvulus microfilaria (4 years)

    Prevalence of O. volvulus microfilaria (mf) is a binary outcome measured by the presence/absence of O. volvulus mf taken from skin snips using Holth corneoscleral punches taken from the buttocks.

    Time frame: 4 years

  2. Community egg load of soil transmitted helminth (STH) eggs (4 years)

    Community egg load is defined as average stool egg count per species. FLOTAC and Kato-Katz (KK) methods will be used to examine a single stool sample from each subject.

    Time frame: 4 years

  3. Prevalence of W. bancrofti microfilaria (7 years)

    Prevalence of W. bancrofti microfilaria (mf) is a binary outcome measured by the presence/absence of W. bancrofti mf in three-line thick smears prepared with a measured 60 microliter quantity of finger prick blood collected between 8pm-2am. The species of mf will be determined by morphological criteria.

    Time frame: 7 years

  4. Prevalence of W. bancrofti filarial antigenemia (7 years)

    Prevalence of this outcome measure is determined by the percentage (%) of individuals with positive tests for the W. bancrofti filarial antigen. Blood will be tested for filarial antigenemia using the Alere Filariasis Test Strip (FTS).

    Time frame: 7 years

  5. Prevalence of O. volvulus microfilaria (7 years)

    Prevalence of O. volvulus microfilaria (mf) is a binary outcome measured by the presence/absence of O. volvulus mf taken from skin snips using Holth corneoscleral punches taken from the buttocks.

    Time frame: 7 years

  6. Community egg load of soil transmitted helminth (STH) eggs (7 years)

    Community egg load is defined as average stool egg count per species. FLOTAC and Kato-Katz (KK) methods will be used to examine a single stool sample from each subject.

    Time frame: 7 years

07

Study locations

1 site
  • Liberian Institute of Biomedical Research
    Charlesville, Margibi, Liberia
08

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Mar 2012 to primary completion in Apr 2017, 61 months.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 12, 2013
First posted
Jul 23, 2013
StartActual
Mar 2012
Primary completionActual
Apr 2017
CompletionActual
Jul 2021
Last update
Feb 11, 2022
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 11, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01905436
Responsible party
Sponsor
First posted
Jul 23, 2013
Start date
Mar 2012
Primary completion
Apr 2017
Completion
Jul 2021
Last update
Feb 11, 2022

Study contacts

Gary J Weil, MD
principal investigator · Washington University School of Medicine
Peter U Fischer, PhD
principal investigator · Washington University School of Medicine
Fatorma K Bolay, PhD
study director · Liberian Institute of Biomedical Research

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Feb 2022. You cannot join it, but the record below documents what was studied.

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