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Clinical Trials/NCT01663831
NCT01663831CompletedNot Applicable

Repellents as Added Control Measure to Long Lasting Insecticidal Nets to Target the Residual Transmission in Southeast Asia: a Step Forwards to Malaria Elimination

Institute of Tropical Medicine, Belgium1 site in 1 country40,000 target enrollmentStarted: May 1, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
40,000
Locations
1
Primary Endpoint
Change from baseline in malaria prevalence at 6 months

Study Overview

Brief Summary

The scaling up of Long Lasting Insecticidal Nets (LLIN) and the expansion of Indoor Residual Spraying (IRS) has contributed to a significant decrease of malaria worldwide. However these control methods tackle only indoor and night biting vectors. The proportion of transmission occurring outdoors and before sleeping hours or so-called "residual transmission" is steadily increasing and may compromise the effort towards malaria elimination.

The purpose of this study is to raise evidence on the effectiveness of mass use of topical repellents in addition to LLINs in controlling malaria infections.

A multidisciplinary approach will be used to collect information on the most important factors that contribute to the successful reduction of "residual malaria transmission". In a first objective the epidemiological efficacy of repellents on prevalence of malaria carriers and malaria incidence will be assessed. To achieve this goal 98 communities will be randomly assigned to one of two treatment arms (LLIN and LLIN + repellent). Within a community a cross sectional random sample of 65 people will be drawn at the beginning and the end of the malaria season to obtain an estimate of the malaria prevalence. The second objective will handle the entomological efficacy and persistence of the topical repellent on malaria vectors. And lastly the acceptability, adherence and adequacy of the topical repellents will be studied in a third objective.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
2 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • All household members volunteering from selected communities

Exclusion Criteria

  • Infants less than 2 years

Arms & Interventions

Topical Repellent & LLIN

Experimental

Intervention: Mosquito topical repellent (Other)

Long Lasting Insecticidal Nets

No Intervention

Brand Name LLIN: Olyset Net

Active ingredient: permethrin

Outcomes

Primary Outcomes

Change from baseline in malaria prevalence at 6 months

Time Frame: 6 months

Malaria prevalence (PCR detection) will be measured in both study arms at the start and end of the malaria season for 2 consecutive years.

Secondary Outcomes

  • Malaria incidence(6 months)

Investigators

Sponsor
Institute of Tropical Medicine, Belgium
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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