Laboratory Testing |
Use 20% deet in ethanol as a positive comparison |
Human subjects preferable to reflect the end user |
Before the test the test area of skin should be washed with unscented soap then rinsed with 70% ethanol / isopropyl alcohol |
Mosquitoes should be reared under standard 27 ± 2 C temperature, ≥80 ± 10% relative humidity, and a 12:12 (light:dark) photoperiod. |
Mosquitoes should be 3 to 5 days old, nulliparous females, starved for 12 hours preceding the test |
Tests should be conducted with three or more species |
40 x 40 x 40 cm cages with 50 – 100 mosquitoes for effective dose testing |
40 x 40 x 40 cm cages with 200 - 250 mosquitoes for complete protection time testing |
Control arms should be used to estimate mosquito readiness to feed |
Treatment arms should be offered to mosquitoes after avidity has been measured |
Field Testing |
Use 20% deet in ethanol as a positive comparison |
Human subjects preferable to reflect the end user |
Before the test the test area of skin should be washed with unscented soap then rinsed with 70% ethanol / isopropyl alcohol |
Volunteers should sit >20 metres apart |
Design should be completely randomised |
Trials should be conducted with medium biting pressures of representative vector species |
All participants should be recruited on informed consent from the local area and be provided with malaria prophylaxis |
In all testing monitoring of adverse effects should be carried out |