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Iron fortification and parasite control to reduce anaemia among schoolchildren in Cote d'Ivoire

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN21782274
Enrollment
640
Registered
2006-11-21
Start date
2006-11-27
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Mild to moderate anaemia Haematological Disorders Anaemia

Interventions

1. Iron fortification (biscuitis with two x 10 mg Fe/day/child
four per week) 2. Intermittent preventative treatment (sulfadoxine (500 mg) and pyrimethamine (25 mg)
three times, interval: three-month) 3. Albendazole (400 mg) and praziquantel (40 mg/kg)
three times, interval: three-month

Sponsors

ETH Food Science and Nutrition (Switzerland)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Child, aged six to 14 years, both sexes, attending the local primary school of five selected villages 2. For girls, not pregnant (as assessed by medical doctor) 3. Absence of major systemic illnesses (as assessed by medical doctor upon initial full clinical assessment) 4. Anticipated residence in the study area for at least one year 5. Mild to moderate anaemia defined as Haemoglobin (Hb) more than 80 g/L and less than 115 g/L in children aged between six and 12 years, and Hb more than 80 g/Land less than 120 g/L in children more than or equal to 12 years 6. No known or reported hypersensitivity to albendazole, praziquantel or sulfadoxine-pyrimethamine 7. No known or reported history of significant chronic illness 8. No known history of anthelmintic treatment in the four weeks prior to study enrolment 9. Written informed consent of parents or legal guardian

Exclusion criteria

Exclusion criteria: 1. Hb less than 80g/L 2. Attending any other clinical trials during the study period 3. Presence of any abnormal medical condition, judged by the investigator medical team

Design outcomes

Primary

MeasureTime frame
1. Reduction in anaemia 2. Change in cognitive performance

Secondary

MeasureTime frame
Number of clinical malaria episodes during trial period

Countries

Cote d'Ivoire

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 6, 2026