Trial | NCT01599000  Report issue

Official Title

Artemether-Lumefantrine Clinical Effectiveness Study

  • Phase

    Phase 4

  • Study Type

    Interventional

  • Status

    Completed No Results Posted

  • Study Participants

    159
In 2009, Papua New Guinea officially adopted artemether-lumefantrine (AL) as new national first-line drug for uncomplicated malaria. The principal purpose of this study is to measure the absolute effectiveness of AL when used under real-life clinical conditions, as compared to optimized in-vivo trial conditions. This question was raised by the National Department of Health in preparation for the country-wide roll-out of AL.

The study is designed as a randomized controlled trial comparing two study arms. Patients in the "effectiveness arm" receive the first dose of AL under full supervision in the clinic; the following doses will be taken at home, as in real-life clinical practice and according to the new national treatment guidelines. Patients in the "efficacy arm" will receive all doses of AL as directly observed treatment in the clinic in order to establish the efficacy of the drug when used under ideal conditions.

The study will enroll outpatients aged 6 months to 10 years with a history of fever and a positive rapid test for malaria. Patients meeting all enrollment criteria and providing full written informed consent by a parent/caretaker will be randomized into either of the two study arms. Patients in both arms will be followed up actively for 42 days. Patients in the efficacy arm will be scheduled for visits on days 0, 1, 2, 3, 7, 14, 28 and 42; patients in the effectiveness arm on days 0, 3, 7, 14, 28 and 42.
Study Started
Mar 31
2011
Primary Completion
Jul 31
2012
Study Completion
Jul 31
2012
Last Update
Aug 16
2012
Estimate

Drug Artemether-lumefantrine combination

fixed-dose tablet, six doses over three days, according to weight group

  • Other names: Coartem, Novartis

Efficacy arm Active Comparator

Supervised administration of six doses of fixed-dose artemether-lumefantrine (Coartem, Novartis)

Effectiveness arm Experimental

Un-supervised administration of six doses of fixed-dose artemether-lumefantrine (Coartem, Novartis)

Criteria 

Inclusion Criteria:

Age 6 months to 10 years (+/- 1 month for children without known date of birth)
Permanent resident in the study area
Not enrolled in another study at the same time
No known history of hypersensitivity reactions to artemether or lumefantrine
History of fever in the previous 72 hours (approximate)
Rapid diagnostic test (RDT) positive for any species of Plasmodium

Exclusion Criteria:

General danger signs: inability to drink or breastfeed, vomiting everything, recent history of convulsions, lethargy or unconsciousness, inability to sit or stand up
Signs of severe malaria (impaired consciousness, respiratory distress, circulatory collapse, abnormal bleeding, jaundice, or as determined by clinician)
Severe malnutrition: defined as a child whose weight-for-height is below -3 standard deviation or less than 70% of the median of the NCHS/WHO normalized reference values, or who has symmetrical oedema involving at least the feet; or middle upper arm circumference under 12 cm
Clinically significant concomitant disease requiring admission
Contraindications mentioned in the national treatment guidelines
No Results Posted