Clinical Trials Directory

Trials / Completed

CompletedNCT01454752

Intermittent Parasite Clearance (IPC) in Schools: Impact on Malaria, Anaemia and Cognition

Intermittent Parasite Clearance (IPC) in Schools: a Randomised Double-blind Placebo-controlled Trial of the Impact of IPC on Malaria, Anaemia and Cognition Amongst School Children in Kedougou, Senegal

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
860 (actual)
Sponsor
London School of Hygiene and Tropical Medicine · Academic / Other
Sex
All
Age
7 Years – 14 Years
Healthy volunteers
Accepted

Summary

Although the risk of malaria is greatest in early childhood, significant numbers of schoolchildren remain at risk from malaria infection, clinical illness and death. By the time they reach school, many children have already acquired some clinical immunity and the ability to limit parasite growth, and thus most infections are asymptomatic and will go undetected and untreated. Asymptomatic parasitaemia contributes to anaemia, reducing concentration and learning in the classroom, and interventions aiming to reduce asymptomatic parasite carriage may bring education, as well as health, benefits. Intermittent parasite clearance (IPC) delivered through schools is a simple intervention, which can be readily integrated into broader school health programmes, and may usefully supplement the community-distribution of insecticide-treated nets (ITNs) in countries with a policy of universal coverage of nets. This study seeks to establish whether intermittent parasite clearance undertaken once a year at the end of the malaria transmission season can reduce malaria parasite carriage and anaemia amongst school-going children already using insecticide-treated nets, and its consequent impact on school attendance and performance, in order to assess its suitability for inclusion as a standard intervention in school health programmes in areas of seasonal malaria transmission.

Conditions

Interventions

TypeNameDescription
DRUGIntermittent parasite clearanceSulphadoxine-pyrimethamine (500/25mg) according to age, given on day 1; Amodiaquine (200mg) according to age, given daily for 3 days
OTHERPlaceboPlacebo tablets, similar in appearance and taste to active treatment, given daily over 3 days

Timeline

Start date
2011-11-01
Primary completion
2012-02-01
Completion
2012-02-01
First posted
2011-10-19
Last updated
2012-04-19

Locations

1 site across 1 country: Senegal

Source: ClinicalTrials.gov record NCT01454752. Inclusion in this directory is not an endorsement.