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Trial registered on ANZCTR
Registration number
ACTRN12613000586718
Ethics application status
Approved
Date submitted
21/05/2013
Date registered
24/05/2013
Date last updated
24/05/2013
Type of registration
Prospectively registered
Titles & IDs
Public title
Updating the efficacy study of artemether-lumefantrine for the treatment of uncomplicated P falciparum malaria in sentinel sites in the Comoros Islands.
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Scientific title
Safety and efficacy, in terms of adequate clinical and parasitological response, of artemether lumefantrine for the treatment of children with uncomplicated P. falciparum malaria in Comoros Islands.
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Secondary ID [1]
282535
0
None
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
uncomplicated falciparum malaria
289202
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Condition category
Condition code
Infection
289532
289532
0
0
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Other infectious diseases
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Therapeutic efficacy study of the fixed combination of artemether-lumefantrine ( 20 mg artemether/ 120 mg lumefantrine) administered orally twice a day for three consecutive days. The number of tablets to be administered at each dosing day will be based on body weight as per standard of care. Patients will be seen daily for the first three days and then return to the health center weekly (day 7, 14, 21 and 28) for clinical and parasitological evaluation or any other day if symptoms re-occurred.
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Intervention code [1]
287201
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Not applicable
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Comparator / control treatment
No control
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
289628
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Proportion of patients with adequate clinical and parasitological response adjusted by PCR (polymerase chain reaction)
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Assessment method [1]
289628
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Timepoint [1]
289628
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Day 28
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Secondary outcome [1]
302889
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Nature and incidence of adverse events as observed by investigators or reported by patients. Clinical laboratory testing may be performed to confirm a diagnosis. Possible adverse events include those know to occur with such antimalarial and include, headache, nausea, abdominal discofort, dizziness.
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Assessment method [1]
302889
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Timepoint [1]
302889
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Day 28
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Eligibility
Key inclusion criteria
Age between 6 months to 11 years (inclusive);
Monoinfection with P falciparum, microscopically confirmed
Parasitaemia between 500-200,000 per microliter (asexual forms)
Axillary temperature equal or greater than 37.5 degrees C;
Able to swallow oral medication;
Capable and willing to fulfill protocol requirements, including the schedule of assessments for the duration of the study;
Provide written informed consent (parent or guardian)
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Minimum age
6
Months
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Maximum age
11
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Presence of general danger and signs in children under 5 years or signs of severe falciparum malaria;
Mixed or mono-infection with another Plasmodium species detected by microscopy;
History of hypersensitivity reactions or contraindications to any of the medicines being tested or used as alternative treatments(s);
Severe malnutrition (per WHO definition);
Presence of febrile conditions due to diseases other than malaria (e.g. measles, acute lower respiratory tract infection, severe diarrhea);
Regular medication, which may interfere with antimalarial pharmacokinetics
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/06/2013
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
560
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
5092
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Comoros
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State/province [1]
5092
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Ngazidja
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Country [2]
5093
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Comoros
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State/province [2]
5093
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Mwali
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Country [3]
5094
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Comoros
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State/province [3]
5094
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Ndzouani
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Funding & Sponsors
Funding source category [1]
287317
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Government body
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Name [1]
287317
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Ministere de la Sante, de la Solidarite et de la Promotion du Genre
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Address [1]
287317
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Centre National de Lutte contre le Paludisme/
C/O Organisation Mondiale de la Sante
Itsambouni
B.P. 435
Moroni, Grande Comore
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Country [1]
287317
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Comoros
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Funding source category [2]
287318
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Other
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Name [2]
287318
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World Health Organisation
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Address [2]
287318
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20 Avenue Appia
1211 Geneva
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Country [2]
287318
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Switzerland
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Primary sponsor type
Government body
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Name
Ministere de la Sante, de la Solidarite et de la Promotion du Genre
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Address
Centre National de Lutte contre le Paludisme/
C/O Organisation Mondiale de la Sante
Itsambouni
B.P. 435
Moroni, Grande Comore
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Country
Comoros
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Secondary sponsor category [1]
286066
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None
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Name [1]
286066
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Address [1]
286066
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Country [1]
286066
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Other collaborator category [1]
277416
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University
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Name [1]
277416
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Institut Pasteur de Madagascar
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Address [1]
277416
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B.P. 1274
Ambatofotsikely
101 Antananarivo
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Country [1]
277416
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Madagascar
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
289290
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WHO ERC
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Ethics committee address [1]
289290
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World Health Organisation 20 Avenue Appia 1211 Geneva
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Ethics committee country [1]
289290
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Switzerland
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Date submitted for ethics approval [1]
289290
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20/03/2013
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Approval date [1]
289290
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14/05/2013
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Ethics approval number [1]
289290
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RPC570
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Summary
Brief summary
Therapeutic efficacy study of the fixed combination of artemether-lumefantrine (20 mg artemether/ 120 mg lumefantrine) administered orally twice a day for three consecutive days. The number of tablets per dosing will be based on body weight per standard of care. Patients will be seen daily for the first three days and then return to the health center weekly (day 7, 14, 21 and 28) for clinical and parasitological evaluation or any other day if symptoms re-occurred.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
40206
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Mrs Rahamatou SILAI
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Address
40206
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Ministere de la Sante, de la Solidarite et de la Promotion du Genre a l'Union des Comores
C/O Organisation Mondiale de la Sante
Itsambouni
B.P. 435
Moroni
Grande Comore
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Country
40206
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Comoros
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Phone
40206
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+2693330375
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Fax
40206
0
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Email
40206
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[email protected]
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Contact person for public queries
Name
40207
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Rahamatou SILAI
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Address
40207
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Ministere de la Sante, de la Solidarite et de la Promotion du Genre a l'Union des Comores
C/O Organisation Mondiale de la Sante
Itsambouni
B.P. 435
Moroni
Grande Comore
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Country
40207
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Comoros
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Phone
40207
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+2693330375
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Fax
40207
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Email
40207
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[email protected]
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Contact person for scientific queries
Name
40208
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Rahamatou SILAI
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Address
40208
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Ministere de la Sante, de la Solidarite et de la Promotion du Genre a l'Union des Comores
C/O Organisation Mondiale de la Sante
Itsambouni
B.P. 435
Moroni
Grande Comore
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Country
40208
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Comoros
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Phone
40208
0
+2693330375
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Fax
40208
0
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Email
40208
0
[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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