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Chloroquine and Coartem for Treatment of Symptomatic Children With Plasmodium Falciparum in Guinea Bissau

Primary Purpose

Malaria, Falciparum

Status
Completed
Phase
Phase 4
Locations
Guinea-Bissau
Study Type
Interventional
Intervention
Chloroquine
Artemether-lumefantrine (Coartem)
Sponsored by
Bandim Health Project
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malaria, Falciparum focused on measuring malaria, Plasmodium falciparum, children, Guinea-Bissau, artemether, lumefantrine, chloroquine, Coartem

Eligibility Criteria

6 Months - 15 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children presenting at one of the health centres in the study area
  • Symptoms suggestive of malaria
  • At least 20 P.falciparum parasites per 200 leucocytes
  • Living in the study area (to enable follow-up)

Exclusion Criteria:

  • Danger signs
  • By the responsible doctor evaluated to need to be transferred to the national hospital as an in-patient
  • Previous idiosyncratic reactions to any of the study drugs

Sites / Locations

  • Bandim Health Project

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1 Coartem

2 Chloroquine

Arm Description

Treatment of documented malaria in children following the dosages recommended by the manufacturer.

The antimalarial actually used in Guinea-Bissau is the dosage of 50 mg/kg given twice a day for 3 days.

Outcomes

Primary Outcome Measures

Parasite reappearance rate,

Secondary Outcome Measures

genetic markers of resistance
recrudescence and re-infection rates
Hospitalisation during follow-up
Haemoglobin changes

Full Information

First Posted
January 23, 2007
Last Updated
January 2, 2011
Sponsor
Bandim Health Project
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1. Study Identification

Unique Protocol Identification Number
NCT00426439
Brief Title
Chloroquine and Coartem for Treatment of Symptomatic Children With Plasmodium Falciparum in Guinea Bissau
Official Title
Chloroquine and Coartem for Treatment of Symptomatic Children With Plasmodium Falciparum in Guinea Bissau.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2011
Overall Recruitment Status
Completed
Study Start Date
December 2006 (undefined)
Primary Completion Date
November 2008 (Actual)
Study Completion Date
November 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Bandim Health Project

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will evaluate the efficacy of treatment with artemether-lumefantrine as compared to chloroquine in the dose of 50 mg/kg for treatment of malaria in children in Guinea-Bissau. The genetic basis of the parasites for developing resistance will be examined. Children coming to one of the Health Centres with symptoms of malaria and a positive malaria test will be included. The children will be followed weekly until day 70. In case of reappearance of parasites the child will be re-treated with the opposite study drug.
Detailed Description
This study compares treatment of uncomplicated malaria in children in Guinea-Bissau with artemether-lumefantrine (Coartem) with that of treatment with chloroquine 50 mg/kg. Furthermore, the genetic basis of anti-malarial resistance in Guinea-Bissau will be studied by analyzing specific single nucleotide polymorphisms in pfcrt and pfmdr1 in blood samples from this in vivo trial. We also intend to study whether the recent report that chloroquine sensitive parasites are selected at recrudescence after Coartem is confirmed in Bissau. Following consent to participate, children visiting one of the Health Centres in the study area with mono-infection with Plasmodium falciparum are by block-randomization allocated to one of the treatment groups. The treatment is given supervised by one of the health workers and malaria film taken on day 2 and 3. The children are visited and malaria films obtained once weekly until day 70. On day seven, 100 microliter of capillary blood are drawn for analyses of analyses of drug concentrations in whole blood. On inclusion and whenever a child has recurrent parasitaemia, a filter-paper blood-sample is collected for later PCR analysis. On the day of inclusion, on day 42 and on day 70 the haemoglobin level is measured. If parasites reappear in 50% or more of at least 40 children in one of the treatment groups this treatment arm should be terminated. During the study parents are recommended to bring the child to the health centre in case of any illness. Participating children will be examined and treated free of charge. The opposite study drug will be used for re-treatment of children in case of recrudescence, and the child will be followed as previously planned. The results from this study could be used for the planning of the recommendations for treatment of malaria in Guinea-Bissau. It will provide the National Malaria Programme with information of the efficacy of Coartem before it is implemented.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malaria, Falciparum
Keywords
malaria, Plasmodium falciparum, children, Guinea-Bissau, artemether, lumefantrine, chloroquine, Coartem

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
1 Coartem
Arm Type
Experimental
Arm Description
Treatment of documented malaria in children following the dosages recommended by the manufacturer.
Arm Title
2 Chloroquine
Arm Type
Active Comparator
Arm Description
The antimalarial actually used in Guinea-Bissau is the dosage of 50 mg/kg given twice a day for 3 days.
Intervention Type
Drug
Intervention Name(s)
Chloroquine
Intervention Description
Chloroquine tablets gives as 50 mg/kg divided into 6 doses giver twice a day for 3 days.
Intervention Type
Drug
Intervention Name(s)
Artemether-lumefantrine (Coartem)
Other Intervention Name(s)
Brand name: Coartem.
Intervention Description
Will be dosed according to the recommendations of WHO. Will be given at time: 0 h, 8 h, 24 h, 36 h,48 h and 60 h. The dosage will be according to bodyweight of the child as follows: 5-14 kg: 1 tablet, 15-24 kg: 2 tablets, 25-34 kg: 3 tablets, < 34 kg: 4 tablets.
Primary Outcome Measure Information:
Title
Parasite reappearance rate,
Time Frame
70 days
Secondary Outcome Measure Information:
Title
genetic markers of resistance
Time Frame
70 days
Title
recrudescence and re-infection rates
Time Frame
70 days
Title
Hospitalisation during follow-up
Time Frame
70 days
Title
Haemoglobin changes
Time Frame
70 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children presenting at one of the health centres in the study area Symptoms suggestive of malaria At least 20 P.falciparum parasites per 200 leucocytes Living in the study area (to enable follow-up) Exclusion Criteria: Danger signs By the responsible doctor evaluated to need to be transferred to the national hospital as an in-patient Previous idiosyncratic reactions to any of the study drugs
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Aaby
Organizational Affiliation
Bandim Health Project
Official's Role
Study Director
Facility Information:
Facility Name
Bandim Health Project
City
Apartado 861
State/Province
Bissau
Country
Guinea-Bissau

12. IPD Sharing Statement

Citations:
PubMed Identifier
25421474
Citation
Jovel IT, Kofoed PE, Rombo L, Rodrigues A, Ursing J. Temporal and seasonal changes of genetic polymorphisms associated with altered drug susceptibility to chloroquine, lumefantrine, and quinine in Guinea-Bissau between 2003 and 2012. Antimicrob Agents Chemother. 2015 Feb;59(2):872-9. doi: 10.1128/AAC.03554-14. Epub 2014 Nov 24.
Results Reference
derived
PubMed Identifier
21148503
Citation
Ursing J, Kofoed PE, Rodrigues A, Blessborn D, Thoft-Nielsen R, Bjorkman A, Rombo L. Similar efficacy and tolerability of double-dose chloroquine and artemether-lumefantrine for treatment of Plasmodium falciparum infection in Guinea-Bissau: a randomized trial. J Infect Dis. 2011 Jan 1;203(1):109-16. doi: 10.1093/infdis/jiq001.
Results Reference
derived

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Chloroquine and Coartem for Treatment of Symptomatic Children With Plasmodium Falciparum in Guinea Bissau

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