Evidence map›Paper›PMID 40140904›Full record

Trial reportInfectious diseases of poverty2025

Collateral benefits of ivermectin mass drug administration designed for malaria against headlice in Mopeia, Mozambique: a cluster randomised controlled trial.

Joanna Furnival-Adams, Amelia Houana, Patricia Nicolas, Julia Montaña, Samuel Martinho, Aina Casellas, Hansel Mundaca, Jenisse Mbanze, Arlindo Soares, Saimado Imputiua and 14 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Infectious diseases of poverty, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04966702 (A Phase III Cluster-randomized, Open-label, Clinical Trial to Study the Safety and Efficacy of Ivermectin Mass Drug Administration to Reduce Malaria Transmission in Two African Settings), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04966702 phase3completednot on this map

A Phase III Cluster-randomized, Open-label, Clinical Trial to Study the Safety and Efficacy of Ivermectin Mass Drug Administration to Reduce Malaria Transmission in Two African Settings

TypeinterventionalSponsorBarcelona Institute for Global HealthRan2022 to 2024Enrolled48,145ConditionsMalariaArmsAlbendazole Pill, Ivermectin Pill, Ivermectin Injectable Product
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Joanna Furnival-AdamsIsGlobal, Barcelona Institute for Global Health, Barcelona, Spain. joannafa28@gmail.com.ORCID http://orcid.org/0000-0002-2451-0107
Amelia HouanaCentro de Investigação em Saúde de Manhiça (Manhica Health Research Centre), Mopeia, Mozambique.
Patricia NicolasIsGlobal, Barcelona Institute for Global Health, Barcelona, Spain.
Julia MontañaIsGlobal, Barcelona Institute for Global Health, Barcelona, Spain.
Samuel MartinhoCentro de Investigação em Saúde de Manhiça (Manhica Health Research Centre), Mopeia, Mozambique.
Aina CasellasIsGlobal, Barcelona Institute for Global Health, Barcelona, Spain.
Hansel MundacaIsGlobal, Barcelona Institute for Global Health, Barcelona, Spain.
Jenisse MbanzeCentro de Investigação em Saúde de Manhiça (Manhica Health Research Centre), Mopeia, Mozambique.
Arlindo SoaresCentro de Investigação em Saúde de Manhiça (Manhica Health Research Centre), Mopeia, Mozambique.
Saimado ImputiuaCentro de Investigação em Saúde de Manhiça (Manhica Health Research Centre), Mopeia, Mozambique.
Paula Ruiz-CastilloIsGlobal, Barcelona Institute for Global Health, Barcelona, Spain.
Marta RibesIsGlobal, Barcelona Institute for Global Health, Barcelona, Spain.
Almudena SanzIsGlobal, Barcelona Institute for Global Health, Barcelona, Spain.
Mussa Mamudo SaléCentro de Investigação em Saúde de Manhiça (Manhica Health Research Centre), Mopeia, Mozambique.
Antonio MacuchaCentro de Investigação em Saúde de Manhiça (Manhica Health Research Centre), Mopeia, Mozambique.
Eldo EloboloboCentro de Investigação em Saúde de Manhiça (Manhica Health Research Centre), Mopeia, Mozambique.
Vegovito VegoveCentro de Investigação em Saúde de Manhiça (Manhica Health Research Centre), Mopeia, Mozambique.
Victor MutepaCentro de Investigação em Saúde de Manhiça (Manhica Health Research Centre), Mopeia, Mozambique.
Humberto MunguambeCentro de Investigação em Saúde de Manhiça (Manhica Health Research Centre), Mopeia, Mozambique.
Aida XerindaCentro de Investigação em Saúde de Manhiça (Manhica Health Research Centre), Mopeia, Mozambique.
Felisbela MaterulaCentro de Investigação em Saúde de Manhiça (Manhica Health Research Centre), Mopeia, Mozambique.
Regina RabinovichIsGlobal, Barcelona Institute for Global Health, Barcelona, Spain.
Francisco SauteCentro de Investigação em Saúde de Manhiça (Manhica Health Research Centre), Mopeia, Mozambique.
Carlos ChaccourIsGlobal, Barcelona Institute for Global Health, Barcelona, Spain.

Funding

Unitaid BOHEMIA
6 · The paper itself

Abstract

backgroundHeadlice are prevalent worldwide, with a higher burden in rural, lower-middle income settings. They can cause intense itchiness, discomfort, and secondary bacterial infections with potentially serious consequences. Ivermectin is efficacious against headlice, and is also being evaluated as a malaria vector control tool. In this study, we explored risk factors for headlice, and assessed the efficacy of ivermectin mass drug administration (MDA) designed for malaria against headlice.

methodsWe conducted an open-label, assessor-blind, cluster-randomized controlled trial in Mopeia, Mozambique. A single dose of ivermectin was given monthly to eligible humans or humans and livestock (humans: 400 μg/kg, livestock: 1% injectable 200 μg/kg) in 3 consecutive months during the rainy season. The control group received albendazole (humans only). Thirty-nine clusters (13 per arm) were randomly selected for the nested assessment of headlice prevalence. 1341 treated participants were followed up at least once, 1, 2 and 3 months and 382 untreated (ineligible) participants at 3 and 6 months after the first MDA round. Headlice diagnosis was determined by scalp examination. Logistic regression was used to identify risk factors for headlice at baseline, and to estimate the treatment effect at each time point.

resultsA total of 1309 participants were included in the main analysis assessing ivermectin MDA efficacy, and 1332 in the risk factor analysis. The baseline headlice prevalence was 11%. Risk factors included living with a household member with head itch [adjusted odds ratio (aOR) = 48.63, 95% confidence interval (CI): 28.7-82.3, P-value < 0.0001], being female (aOR = 2.25, 95% CI: 1.33-3.80, P-value < 0.01), and using surface water as the main water (aOR = 2.37, 95% CI: 1.12-5.33, P-value = 0.04). The treated population receiving ivermectin had significantly lower odds of having headlice at 3 months compared to those receiving albendazole (aOR = 0.19, 95% CI: 0.04-0.91, P-value = 0.04). There was no indirect effect on headlice among children ineligible for treatment.

conclusionsIn a highly endemic setting, mass drug administration with ivermectin significantly reduces headlice infestation prevalence among those who receive the drug for three sequential months. The lack of effect among untreated, ineligible children implies that additional interventions would be needed to interrupt local transmission.

trial registrationThis study is registered with ClinicalTrials.gov (NCT04966702).

Indexed as

Antiparasitic AgentsIvermectinMalariaMass Drug AdministrationPediculusScalp DermatosesAdolescentAdultAnimalsChildChild, PreschoolFemaleHumansInfantMaleMiddle AgedAntiparasitic AgentsIvermectinEctoparasitesHeadliceIvermectinMalariaMass drug administration

Identifiers

PMID40140904
PMCPMC11948683

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.