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The Combined Use of Indoor Residual Spraying (IRS) and Long-lasting Insecticidal Nets (LLINs) for Malaria Prevention

Cluster Randomised Trial to Compare Effectiveness of the Combined Use of Indoor Residual Spraying (IRS) and Long-lasting Insecticidal Nets (LLINs) to LLINs Alone for Malaria Prevention in Muleba District, Kagera Region, Tanzania

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01697852
Enrollment
22300
Registered
2012-10-02
Start date
2011-01-31
Completion date
2012-12-31
Last updated
2012-10-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malaria

Keywords

vector control, LLIN, IRS

Brief summary

The study is a cluster randomised trial to compare the effectiveness of indoor residual spraying (IRS) combined with the use of long lasting insecticidal nets (LLINs) with the effectiveness of LLINs alone for preventing malaria infection and morbidity. The primary outcome measure is prevalence of parasitaemia and anaemia in children aged 0.5-10 years, measured in cross sectional surveys. Secondary outcomes include relative population density for each mosquito vector species, malaria transmission as measured by entomological inoculation rates (EIR) by mosquito vector species, monitoring of resistance markers including kdr, and user acceptability of LLINs compared with IRS. Findings from this study are expected to inform decision making so that resource utilization can be optimised.

Interventions

OTHERIndoor residual spraying with bendiocarb

2 rounds of indoor residual spraying with bendiocarb insecticide, 4 months apart

OTHERLLIN by universal coverage campaign

Long lasting Insecticide treated mosquito net

Sponsors

National Institute for Medical Research, Tanzania
CollaboratorOTHER_GOV
Kilimanjaro Christian Medical Centre, Tanzania
CollaboratorOTHER
London School of Hygiene and Tropical Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Months to 14 Years
Healthy volunteers
Yes

Inclusion criteria

* resident in selected cluster (village)

Exclusion criteria

* Not resident in selected cluster (village)

Design outcomes

Primary

MeasureTime frame
Prevalence of malarial infection in children 6 months to 10 years9 months post randomisation

Secondary

MeasureTime frame
Moderate to severe anaemia in children under 5 years9 months post randomisation
Post-spraying prevalence of infection with malarial parasites in children 6 months to 10 years6 months post randomisation

Other

MeasureTime frame
Entomological Innoculation RateMalaria season post randomisation(Average value during 6 months after randomisation)
Relative abundance of adult Anopheles mosquitoes by speciesMalaria season post randomisation (Average value during 6 months after randomisation)
genotypic markers of insecticide resistance in malaria vector mosquitoesMalaria season post randomisation (Average value during 6 months after randomisation)

Countries

Tanzania

Contacts

Primary ContactMark Rowland, PHD
Mark.Rowland@lshtm.ac.uk
Backup ContactImmo Kleinschmidt, PHD
Immo.Kleinschmidt@lshtm.ac.uk

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026