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The Africa Quinine versus Artesunate in Severe Malaria Trial

The AQUAMAT trial: An open label randomised comparison of injectable artesunate and quinine in children with severe falciparum malaria in Africa

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN50258054
Enrollment
5300
Registered
2005-07-22
Start date
2005-10-08
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

Malaria Infections and Infestations Malaria

Interventions

Please note that as of 01/09/10 this trial has reached its target sample size and recruitment has been closed. The trial is now in follow-up. Current information as of 26/01/2009: Patients are rando

Sponsors

University of Oxford (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. OptiMal malaria rapid test positive, and 2. Treating physician considers patient to have severe malaria

Exclusion criteria

Exclusion criteria: 1. Patient has received more than or equal to 24 hours of effective treatment with quinine or an artemisinin derivative, or 2. Patient has a known allergy to quinine or an artemisinin derivative

Design outcomes

Primary

MeasureTime frame
In-hospital mortality

Secondary

MeasureTime frame
Current information as of 20/04/2010: 1. Neurological sequelae at day 28 after discharge from the hospital 2. Combined in-hospital mortality and neurological sequelae at day 28 after discharge from the hospital Initial information at time of registration: 1. Neurological sequelae 2. Recovery times: 2.1. To localise pain 2.2. To speak 2.3. To sit unsupported 2.4. To eat or breast feed, and 2.5. To discharge from hospital Assessed at discharge.

Countries

Congo, Democratic Republic, Gambia, Ghana, Kenya, Mozambique, Nigeria, Rwanda, Tanzania, Uganda

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 30, 2026