Overview

Effectiveness of Oral Quinine and Artemether-Lumefantrine in the Treatment of Uncomplicated Malaria in Ugandan Children

Status:
Unknown status
Trial end date:
2008-04-01
Target enrollment:
0
Participant gender:
All
Summary
We will test the hypothesis that there is a difference in effectiveness of oral quinine in comparison to artemether Lumefantrine in the treatment of uncomplicated malaria in children.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Makerere University
Collaborators:
Ministry of Health, Uganda
Uganda Malaria Surveillance Project
Treatments:
Artemether
Artemether-lumefantrine combination
Artemether, Lumefantrine Drug Combination
Artemisinins
Lumefantrine
Quinine
Criteria
Inclusion Criteria:

1. Aged between 6 and 59 months of age seen at the assessment centre during the study
period

2. With fever defined as axillary temperature ≥37.5 °C or history of fever in the past 24
h

3. With a microscopically confirmed monoinfection of Plasmodium falciparum

4. Able to tolerate oral therapy,

5. Whose parents/guardians have provided written informed consent.

Exclusion Criteria:

1. Children with a history of allergy to quinine, artemether-Lumefantrine or milk.

2. Evidence of severe malaria.

3. Residence at more than 20km from the health clinic.

4. Evidence of a significant concomitant febrile illness that would require
hospitalization or chronic medical illness