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Malaria, Cerebral clinical trials

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NCT ID: NCT00292942 Completed - Malaria Clinical Trials

Study of the Safety of Intravenous Artesunate

Start date: June 12, 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to establish the safety, tolerability, and pharmacokinetics of a multiple dose of the antimalarial drug artesunate.

NCT ID: NCT00292929 Completed - Malaria Clinical Trials

Study of the Safety of Intravenous Artesunate

Start date: n/a
Phase: Phase 1
Study type: Interventional

The purpose of this study is to establish the safety, tolerability and pharmacokinetics of a single dose of the antimalarial drug artesunate.

NCT ID: NCT00124267 Active, not recruiting - Cerebral Malaria Clinical Trials

Efficacy of Intrarectal Versus Intravenous Quinine for the Treatment of Childhood Cerebral Malaria

Start date: September 2003
Phase: Phase 3
Study type: Interventional

Cerebral malaria is the most lethal complication of P.falciparum infection with a mortality rate between 5 and 40%. Intravenous quinine remains the recommended treatment for cerebral malaria. However its administration is often not feasible due to lack of simple equipment or trained staff. When referral is not possible, a viable alternative is needed. The intrarectal route is of interest in children since it is painless and simple. Studies of the efficacy of intrarectal quinine in the treatment of cerebral malaria are limited. The study aims to establish the efficacy of intrarectal quinine in the treatment of childhood cerebral malaria.

NCT ID: NCT00113854 Active, not recruiting - Cerebral Malaria Clinical Trials

Mannitol as Adjunct Therapy for Childhood Cerebral Malaria

Start date: October 2004
Phase: Phase 3
Study type: Interventional

Cerebral malaria is a life-threatening complication of Plasmodium falciparum infection in African children and nonimmune travellers despite availability of quinine, the current drug of choice. Several reports have suggested that raised intracranial pressure (ICP) is a major cause of death among children with cerebral malaria. Mannitol, an osmotic diuretic, effectively lowers ICP and is used to treat post traumatic raised ICP. There have been some case reports of reduction in mortality and morbidity in African children with cerebral malaria following administration of mannitol, but as these were not randomized controlled trials it is difficult to evaluate their significance. This study seeks to establish whether a single dose of intravenous mannitol given to children with cerebral malaria will significantly reduce the coma recovery time.