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Treatment of Uncomplicated Childhood Malaria in Tanzania by Artemether+Lumefantrine - Efficacy and Genotyping

Primary Purpose

Malaria

Status
Completed
Phase
Phase 4
Locations
Tanzania
Study Type
Interventional
Intervention
artemether-lumefantrine
Sponsored by
Karolinska University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malaria

Eligibility Criteria

1 Year - 10 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age 1-10 years Presence of asexual P. falciparum parasitaemia of 2000-200 000/μL No general danger signs or severe malaria present Haemoglobin ≥70 g/L History of fever within 24 hours OR axillary temperature ≥ 37.5Cº No other cause of fever is detectable No severe malnutrition Guardian/patient has understood the procedures of the study and willing to participate Exclusion Criteria: Not able to drink or breastfeed Vomiting everything Recent history of convulsions Lethargic or unconscious Unable to sit or stand (as appropriate for age) History of allergy to test drugs History of intake of any drugs other than paracetamol and aspirin within 3 days Symptoms/signs of severe malaria

Sites / Locations

  • Fukayosi Primary Health Care Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

All treatment doses accompanied with intake of fatty food

All treatment doses not-accompanied with intake of fatty food.

Outcomes

Primary Outcome Measures

Number of P.falciparum genotypes identified at baseline compared with accumulated number of genotypes in all blood samples

Secondary Outcome Measures

Clearance kinetics of P. falciparum measured with PCR genotyping compared with blood slide reading

Full Information

First Posted
June 12, 2006
Last Updated
October 31, 2007
Sponsor
Karolinska University Hospital
Collaborators
Muhimbili University of Health and Allied Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT00336375
Brief Title
Treatment of Uncomplicated Childhood Malaria in Tanzania by Artemether+Lumefantrine - Efficacy and Genotyping
Official Title
Treatment of Uncomplicated Childhood Malaria by an Artemisinin Derivative in Combination With Lumefantrine. Efficacy, Safety and Genotyping.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2007
Overall Recruitment Status
Completed
Study Start Date
June 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
July 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Karolinska University Hospital
Collaborators
Muhimbili University of Health and Allied Sciences

4. Oversight

5. Study Description

Brief Summary
The purpose of this explorative clinical trial is to study parasite population dynamics, diversity and clearance kinetics of Plasmodium falciparum as well as determination of the molecular mechanisms associated with drug resistance during the early phase of artemether-lumefantrine treatment when the drug intake is either accompanied with or without intake of fatty food. The hypothesis is that intake of fatty food together with artemether-lumefantrine will enhance parasite clearance and thereby decrease the risk of early selection of genetic markers related to drug resistance. The study population is children aged 1-10 years with uncomplicated malaria in Bagamoyo District, Tanzania. Enrolled children will be randomly allocated to either intake of a fatty meal or not together with the study drug. Artemether-lumefantrine will be given twice daily for 3 days in standard doses according to bodyweight. Study participants will be admitted during the study period (3 days)to allow close supervision and detailed blood sampling.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malaria

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
All treatment doses accompanied with intake of fatty food
Arm Title
2
Arm Type
Active Comparator
Arm Description
All treatment doses not-accompanied with intake of fatty food.
Intervention Type
Drug
Intervention Name(s)
artemether-lumefantrine
Other Intervention Name(s)
All drug doses of artemether-lumefantrine is given either accompanied with or not-accompanied with intake of fatty food
Intervention Description
All treatment doses given either accompanied or not-accompanied with intake of fatty food.
Primary Outcome Measure Information:
Title
Number of P.falciparum genotypes identified at baseline compared with accumulated number of genotypes in all blood samples
Time Frame
72 hours
Secondary Outcome Measure Information:
Title
Clearance kinetics of P. falciparum measured with PCR genotyping compared with blood slide reading
Time Frame
72 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 1-10 years Presence of asexual P. falciparum parasitaemia of 2000-200 000/μL No general danger signs or severe malaria present Haemoglobin ≥70 g/L History of fever within 24 hours OR axillary temperature ≥ 37.5Cº No other cause of fever is detectable No severe malnutrition Guardian/patient has understood the procedures of the study and willing to participate Exclusion Criteria: Not able to drink or breastfeed Vomiting everything Recent history of convulsions Lethargic or unconscious Unable to sit or stand (as appropriate for age) History of allergy to test drugs History of intake of any drugs other than paracetamol and aspirin within 3 days Symptoms/signs of severe malaria
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anders Bjorkman, Professor
Organizational Affiliation
Karolinska University Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Fukayosi Primary Health Care Center
City
Fukayosi
State/Province
Bagamoyo District
Country
Tanzania

12. IPD Sharing Statement

Citations:
PubMed Identifier
30860013
Citation
Mwaiswelo R, Ngasala B, Jovel I, Xu W, Larsson E, Malmberg M, Gil JP, Premji Z, Mmbando BP, Martensson A. Prevalence of and Risk Factors Associated with Polymerase Chain Reaction-Determined Plasmodium falciparum Positivity on Day 3 after Initiation of Artemether-Lumefantrine Treatment for Uncomplicated Malaria in Bagamoyo District, Tanzania. Am J Trop Med Hyg. 2019 May;100(5):1179-1186. doi: 10.4269/ajtmh.18-0729.
Results Reference
derived
PubMed Identifier
22185672
Citation
Carlsson AM, Ngasala BE, Dahlstrom S, Membi C, Veiga IM, Rombo L, Abdulla S, Premji Z, Gil JP, Bjorkman A, Martensson A. Plasmodium falciparum population dynamics during the early phase of anti-malarial drug treatment in Tanzanian children with acute uncomplicated malaria. Malar J. 2011 Dec 20;10:380. doi: 10.1186/1475-2875-10-380.
Results Reference
derived

Learn more about this trial

Treatment of Uncomplicated Childhood Malaria in Tanzania by Artemether+Lumefantrine - Efficacy and Genotyping

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