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Safety and Efficacy of Methylene Blue Combined With Amodiaquine or Artesunate for Malaria Treatment in Children of Burkina Faso

This study has been completed.
Information provided by:
Heidelberg University Identifier:
First received: October 16, 2007
Last updated: February 2, 2009
Last verified: February 2009
The purpose of the study is to investigate the safety and efficacy profile of a new paediatric MB formulation combined with AQ or AS and compared to AS-AQ in young African children with uncomplicated falciparum malaria.

Condition Intervention Phase
Malaria Drug: Methylenblue-Amodiaquine (MB-AQ) Drug: Methylenblue-Artesunate (MB-AS) Drug: Artesunate-Amodiaquine (AS-AQ) Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Safety and Efficacy of Methylene Blue Combined With Amodiaquine or Artesunate for Malaria Treatment in Children of Burkina Faso: RCT in the Frame of the A8 Project of SFB 544

Resource links provided by NLM:

Further study details as provided by Heidelberg University:

Primary Outcome Measures:
  • Incidence of observed and self-reported non-serious adverse events over the 28 days observation period [ Time Frame: 28 days ]

Secondary Outcome Measures:
  • Incidence of serious adverse events (SAE) and the adequate clinical and parasitological response rate (ACPR) [ Time Frame: 28 days ]
  • Early treatment failure (ETF) rate [ Time Frame: 28 days ]
  • Late clinical failure (LCF) rate at D14 and D28 [ Time Frame: 28 days ]
  • Late parasitological failure (LPF) rate at D14 and D28 [ Time Frame: 28 days ]
  • Fever clearance time [ Time Frame: 28 days ]
  • Parasite clearance time [ Time Frame: 28 days ]
  • Change in haematocrit after 2,14 and 28 days compared to baseline [ Time Frame: 28 days ]
  • MB whole blood concentrations on D3,5 or 7 compared to concentrations after the first dose [ Time Frame: 28 days ]

Estimated Enrollment: 186
Study Start Date: July 2007
Estimated Study Completion Date: October 2007
Arms Assigned Interventions
Active Comparator: 1-Methylenblue-Amodiaquine Drug: Methylenblue-Amodiaquine (MB-AQ)
For 3 days twice daily 10 mg/kg MB accompanied by once daily 10 mg/kg AQ
Active Comparator: 2-Methylenblue-Artesunate Drug: Methylenblue-Artesunate (MB-AS)
3 days once daily 4 mg/kg AS accompanied by twice daily 10 mg/kg MB given over 7 days
Active Comparator: 3-Artesunate-Amodiaquine Drug: Artesunate-Amodiaquine (AS-AQ)
For 3 days once daily 10 mg/kg AQ accompanied by 4mg/kg AS.


Ages Eligible for Study:   6 Months to 59 Months   (Child)
Sexes Eligible for Study:   All

Inclusion Criteria:

  • 0.5-5 year (6-59 months) old children
  • uncomplicated malaria caused by P. falciparum
  • asexual parasites ≥ 2000/µ and ≤ 200000/µ
  • axillary temperature ≥ 37.5 Celsius or a history of fever during last 24 hours
  • Burkinabe nationality
  • informed consent

Exclusion Criteria:

  • complicated or severe malaria
  • any apparent significant disease
  • anaemia (haematocrit < 21%)
  • treated in the same trial before
  • modern antimalarial treatment prior to inclusion (last three days), except children having been treated with chloroquine
  Contacts and Locations
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Please refer to this study by its identifier: NCT00545935

Burkina Faso
Centre de Recherche en Sante de Nouna
Nouna, Burkina Faso
Sponsors and Collaborators
Heidelberg University
Principal Investigator: Olaf Mueller, Prof. Heidelberg University
  More Information Identifier: NCT00545935     History of Changes
Other Study ID Numbers: MB-2007b
Study First Received: October 16, 2007
Last Updated: February 2, 2009

Additional relevant MeSH terms:
Protozoan Infections
Parasitic Diseases
Methylene Blue
Antiprotozoal Agents
Antiparasitic Agents
Anti-Infective Agents
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action processed this record on June 23, 2017