Treatment of Non-falciparum Malaria
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ClinicalTrials.gov Identifier: NCT00725777 |
Recruitment Status :
Completed
First Posted : July 30, 2008
Last Update Posted : February 17, 2012
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Acute Non-falciparum Malaria | Drug: artemether-lumefantrine | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 40 participants |
Allocation: | N/A |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Efficacy and Safety of Artemether Lumefantrine Combination Therapy for the Treatment of Malaria Due to Plasmodium Ovale, Plasmodium Malariae, and Mixed Plasmodium Infections in Gabon |
Study Start Date : | July 2008 |
Actual Primary Completion Date : | December 2011 |
Actual Study Completion Date : | February 2012 |
Arm | Intervention/treatment |
---|---|
Experimental: A |
Drug: artemether-lumefantrine
Standard artemether-lumefantrine treatment |
- Parasitological cure rate on day 28 [ Time Frame: D28 ]
- Frequency and severity of drug related adverse events [ Time Frame: D28 ]

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Ages Eligible for Study: | 6 Months to 60 Years (Child, Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Male or female patients between the age of 6 months and 60 years and with a minimum of 5kg bodyweight
- Presence of uncomplicated malaria confirmed by: i)fever or history of fever in the previous 4 days, and ii)positive microscopy of P. malariae or P. ovale or mixed infection with P.falciparum with parasite density > 50-200000/μl of blood
- Written informed consent
Exclusion Criteria:
- Patients with presence of other clinical conditions requiring hospitalization
- Presence of other febrile conditions
- Presence of significant anemia, defined by hemoglobin < 7g/dl
- Known history of hypersensitivity,allergic or adverse reactions to artemether or lumefantrine
- Intake of any antimalarial or antibiotics with known antimalarial activity in the preceding 2 weeks
- Pregnant and breast feeding females

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00725777
Gabon | |
Medical Research Unit of the Albert Schweitzer Hospital | |
Lambaréné, Moyen Ogooue, Gabon, BP 118 |
Principal Investigator: | Sabine Bélard, MD | Medical Research Unit of the Albert Schweitzer Hospital in Lambaréné |
Responsible Party: | Michael Ramharter, Ass. Prof. PD, Albert Schweitzer Hospital |
ClinicalTrials.gov Identifier: | NCT00725777 |
Other Study ID Numbers: |
IDC-08-01 |
First Posted: | July 30, 2008 Key Record Dates |
Last Update Posted: | February 17, 2012 |
Last Verified: | February 2012 |
Malaria Protozoan Infections Parasitic Diseases Infections Vector Borne Diseases Lumefantrine |
Artemether Artemether, Lumefantrine Drug Combination Antimalarials Antiprotozoal Agents Antiparasitic Agents Anti-Infective Agents |