search
Back to results

Randomized Trial on Effectiveness of ACTs in Ghana

Primary Purpose

Malaria, Falciparum

Status
Terminated
Phase
Phase 4
Locations
Ghana
Study Type
Interventional
Intervention
Artesunate plus Amodiaquine
Artemether-Lumefantrine
Sponsored by
Bernhard Nocht Institute for Tropical Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malaria, Falciparum focused on measuring Ghana, Effectiveness, Safety, Drug-Resistance, ACT, Coartem, Arsucam

Eligibility Criteria

6 Months - 59 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male and female outpatients aged 6 months to 59 months
  • Absence of severe malnutrition
  • A slide-confirmed P. falciparum asexual parasitaemia between 2,000/µl and 200,000/µl
  • A measured axillary temperature ≥ 37.5 °C or rectal/tympanic temperature ≥ 38.0 °C
  • Absence of general danger signs (unable to drink; repeated vomiting; recent history of convulsions; lethargic or unconscious state; unable to stand up or to sit)
  • Ability to tolerate oral therapy
  • Permanent residence in study area
  • Informed consent by the legal representative of the subject, if possible, the parents

Exclusion Criteria:

  • Adequate anti-malarial treatment within the previous 7 days
  • Antibiotic treatment for a current infection
  • Previous participation in a clinical trial
  • Haemoglobin < 5 g/dl
  • Leucocyte count: > 15000/µl
  • Mixed plasmodial infection
  • Severe malaria as defined by WHO recommendations
  • Any other severe underlying disease (cardiac, renal, hepatic diseases, malnutrition, known HIV infection) or concomitant disease masking assessment of response
  • History of allergy or intolerance against trial medication

Sites / Locations

  • Agogo Presbyterian Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

AL

ASAQ

Arm Description

Artemether plus Lumefantrine 6 dose 3 days treatment

Artesunate plus Amodiaquine

Outcomes

Primary Outcome Measures

Clinical and PCR-controlled parasitological cure rate at day 28

Secondary Outcome Measures

Clinical and PCR-controlled parasitological cure rate at day 14
Effect on anaemia
Molecular Drug Resistance Markers
Recrudescence and Reinfection
Effects on Gametocytemia
Acceptance of Therapies
Incidences of malaria episodes over a follow-up period of 1 year

Full Information

First Posted
September 8, 2006
Last Updated
November 26, 2007
Sponsor
Bernhard Nocht Institute for Tropical Medicine
Collaborators
Presbyterian Health Service (PHS), Kumasi Centre for Collaborative Research (KCCR), School of Medical Sciences Kumasi (SMS/KNUST)
search

1. Study Identification

Unique Protocol Identification Number
NCT00374205
Brief Title
Randomized Trial on Effectiveness of ACTs in Ghana
Official Title
A Comparative Assessment of the Effectiveness of Artemether Plus Lumefantrine Versus Artesunate Plus Amodiaquine for the Treatment of Children With Uncomplicated Plasmodium Falciparum Malaria
Study Type
Interventional

2. Study Status

Record Verification Date
November 2007
Overall Recruitment Status
Terminated
Why Stopped
Interim analysis showed more LCFs in one of the treatment arms
Study Start Date
September 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
October 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Bernhard Nocht Institute for Tropical Medicine
Collaborators
Presbyterian Health Service (PHS), Kumasi Centre for Collaborative Research (KCCR), School of Medical Sciences Kumasi (SMS/KNUST)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare the effectiveness and safety of two Artemisinin Combination Therapies (ACTs) for the treatment of children with uncomplicated Plasmodium falciparum malaria
Detailed Description
Childhood mortality related to Plasmodium falciparum malaria is on the rise with more than 1 million deaths per year in Sub-Saharan Africa. In the context of growing drug-resistance to antimalarials health officials are calling for rapid replacement of failing drugs by combining antimalarial drugs. Artemisinin Combination Antimalarial Therapies (ACTs) are in the focus of malaria control programmes and are recommended for first-line treatment in African countries. ACTs have been reported to be highly effective as artemisinin derivatives cause a rapid and substantial decrease in the parasite load when used for treating patients with malaria and resistance to artemisinin is still lacking. However, the short half-lives of artemisinins result in frequent recrudescent infections when used alone and therefore, much interest lays on the choice of the combination partner drug. ACTs also have been proposed as a means of reducing transmission by the reduction of gametocytes and of delaying the spread of drug resistance and prolonging the therapeutic life span of. Nevertheless, drug resistance of parasites to the respective partner drug is a matter of concern. Artesunate-amodiaquine (AQ) and artemether-lumefantrine (AL) are two registered fixed-dose artemisinin combination chemotherapies used in Africa which are GMP-manufactured at industrial scale. There is still limited data from randomised, controlled trials to support the general effectiveness of these two ACTs in Africa, including Ghana. More data is needed to compare these two therapies to make evidence-based first-line treatment decisions. Importantly, it is difficult to predict how combination therapy may affect the spread of drug resistance and monitoring drug resistance markers should be embedded in these trials to guide drug policy decision. The aim of this open-labelled, randomised drug trial is to compare the effectiveness and safety of artesunate-amodiaquine (Arsucam®) against artemether plus lumefantrine (Coartem®) for the treatment of children under five years of age with uncomplicated Plasmodium falciparum malaria.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malaria, Falciparum
Keywords
Ghana, Effectiveness, Safety, Drug-Resistance, ACT, Coartem, Arsucam

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
AL
Arm Type
Experimental
Arm Description
Artemether plus Lumefantrine 6 dose 3 days treatment
Arm Title
ASAQ
Arm Type
Active Comparator
Arm Description
Artesunate plus Amodiaquine
Intervention Type
Drug
Intervention Name(s)
Artesunate plus Amodiaquine
Other Intervention Name(s)
Arsucam®
Intervention Description
Artesunate 50 mg and Amodiaquine 153 mg co-blister tablets: 3 days once daily weight-adjusted dosing according to manufacturer
Intervention Type
Drug
Intervention Name(s)
Artemether-Lumefantrine
Other Intervention Name(s)
Coartem®
Intervention Description
Artemether 20 mg/Lumefantrine 120mg fixe-dose-combination tablets: 3 days twice daily weight-adjusted dosing according to manufacturer
Primary Outcome Measure Information:
Title
Clinical and PCR-controlled parasitological cure rate at day 28
Time Frame
28 days
Secondary Outcome Measure Information:
Title
Clinical and PCR-controlled parasitological cure rate at day 14
Time Frame
14 days
Title
Effect on anaemia
Time Frame
28 days
Title
Molecular Drug Resistance Markers
Time Frame
28 days
Title
Recrudescence and Reinfection
Time Frame
28 days
Title
Effects on Gametocytemia
Time Frame
28 days
Title
Acceptance of Therapies
Time Frame
7 days
Title
Incidences of malaria episodes over a follow-up period of 1 year
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
59 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male and female outpatients aged 6 months to 59 months Absence of severe malnutrition A slide-confirmed P. falciparum asexual parasitaemia between 2,000/µl and 200,000/µl A measured axillary temperature ≥ 37.5 °C or rectal/tympanic temperature ≥ 38.0 °C Absence of general danger signs (unable to drink; repeated vomiting; recent history of convulsions; lethargic or unconscious state; unable to stand up or to sit) Ability to tolerate oral therapy Permanent residence in study area Informed consent by the legal representative of the subject, if possible, the parents Exclusion Criteria: Adequate anti-malarial treatment within the previous 7 days Antibiotic treatment for a current infection Previous participation in a clinical trial Haemoglobin < 5 g/dl Leucocyte count: > 15000/µl Mixed plasmodial infection Severe malaria as defined by WHO recommendations Any other severe underlying disease (cardiac, renal, hepatic diseases, malnutrition, known HIV infection) or concomitant disease masking assessment of response History of allergy or intolerance against trial medication
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel Ansong, MD
Organizational Affiliation
School of Medical Science (SMS), Kwame Nkrumah University of Science and Technology (KNUST), Kumasi, Ghana
Official's Role
Principal Investigator
Facility Information:
Facility Name
Agogo Presbyterian Hospital
City
Agogo
State/Province
Asante Akim North District
Country
Ghana

12. IPD Sharing Statement

Citations:
PubMed Identifier
16871329
Citation
Bukirwa H, Yeka A, Kamya MR, Talisuna A, Banek K, Bakyaita N, Rwakimari JB, Rosenthal PJ, Wabwire-Mangen F, Dorsey G, Staedke SG. Artemisinin combination therapies for treatment of uncomplicated malaria in Uganda. PLoS Clin Trials. 2006 May;1(1):e7. doi: 10.1371/journal.pctr.0010007. Epub 2006 May 19.
Results Reference
background
PubMed Identifier
15850631
Citation
Mutabingwa TK, Anthony D, Heller A, Hallett R, Ahmed J, Drakeley C, Greenwood BM, Whitty CJ. Amodiaquine alone, amodiaquine+sulfadoxine-pyrimethamine, amodiaquine+artesunate, and artemether-lumefantrine for outpatient treatment of malaria in Tanzanian children: a four-arm randomised effectiveness trial. Lancet. 2005 Apr 23-29;365(9469):1474-80. doi: 10.1016/S0140-6736(05)66417-3.
Results Reference
background
PubMed Identifier
16760509
Citation
Makanga M, Premji Z, Falade C, Karbwang J, Mueller EA, Andriano K, Hunt P, De Palacios PI. Efficacy and safety of the six-dose regimen of artemether-lumefantrine in pediatrics with uncomplicated Plasmodium falciparum malaria: a pooled analysis of individual patient data. Am J Trop Med Hyg. 2006 Jun;74(6):991-8.
Results Reference
background
PubMed Identifier
16652314
Citation
Price RN, Uhlemann AC, van Vugt M, Brockman A, Hutagalung R, Nair S, Nash D, Singhasivanon P, Anderson TJ, Krishna S, White NJ, Nosten F. Molecular and pharmacological determinants of the therapeutic response to artemether-lumefantrine in multidrug-resistant Plasmodium falciparum malaria. Clin Infect Dis. 2006 Jun 1;42(11):1570-7. doi: 10.1086/503423. Epub 2006 Apr 26.
Results Reference
background
PubMed Identifier
16163624
Citation
Martensson A, Stromberg J, Sisowath C, Msellem MI, Gil JP, Montgomery SM, Olliaro P, Ali AS, Bjorkman A. Efficacy of artesunate plus amodiaquine versus that of artemether-lumefantrine for the treatment of uncomplicated childhood Plasmodium falciparum malaria in Zanzibar, Tanzania. Clin Infect Dis. 2005 Oct 15;41(8):1079-86. doi: 10.1086/444460. Epub 2005 Sep 13.
Results Reference
background
PubMed Identifier
16845638
Citation
Sidhu AB, Uhlemann AC, Valderramos SG, Valderramos JC, Krishna S, Fidock DA. Decreasing pfmdr1 copy number in plasmodium falciparum malaria heightens susceptibility to mefloquine, lumefantrine, halofantrine, quinine, and artemisinin. J Infect Dis. 2006 Aug 15;194(4):528-35. doi: 10.1086/507115. Epub 2006 Jul 11.
Results Reference
background
Links:
URL
http://www.kccr.de/kccr/
Description
Homepage of the Kumasi Centre for Collaborative Research (study site)

Learn more about this trial

Randomized Trial on Effectiveness of ACTs in Ghana

We'll reach out to this number within 24 hrs