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Clinical Trials/ACTRN12613000627752
ACTRN12613000627752
Not yet recruiting
未知

Efficacy and safety of the fixed combinations of artemether-lumefantrine and artesunate-amodiaquine for the treatment of uncomplicated Plasmodium falciparum malaria in sentinel sites of Melen (Estuary) and of Franceville (Haut Ogooue) in Gabon

PNLP Ministere de la Sante GABO0 sites288 target enrollmentMay 31, 2013

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
PNLP Ministere de la Sante GABO
Enrollment
288
Status
Not yet recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 31, 2013
End Date
TBD
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
PNLP Ministere de la Sante GABO

Eligibility Criteria

Inclusion Criteria

  • Axillary temperature equal or greater than 37\.5 degrees Celsius or history of fever in the past 24 hours.
  • Parasitemia, asexual forms between 2000 and 200 000 per microliter of blood.
  • Mono\-infection with plasmodium falciparum confirmed by microscopy.
  • Age between 12 months and 12 years.
  • Body weight greater than 5 kg.
  • Absence of clinical signs of severe malaria
  • Absence of known serious chronic disease.
  • Absence of severe malnutrition.
  • Capacity to swallow oral medication.
  • Capable and willing to follow protocol requirement including schedule of assessments

Exclusion Criteria

  • Presence of general danger signs in children aged under 5 years, or signs of severe falciparum malaria according to WHO definition.
  • Mixed or mono\-infection with another Plasmodium species detected by microscopy.
  • Presence of severe malnutrition (defined as a child whose growth standard is below minus 3z\-score, has symmetrical oedema involving at least the feet, or has mid\-upper arm circumference less than 110 mm.
  • Presence of febrile conditions due to diseases other than malaria (measles, acute lowest respiratory tract infection, severe dirrhoea with dehydration) or other known underlyning chronic diseases (cardiac, renal and hepatic diseases, HIV/AIDS).
  • Regular medication, which may interfere with animalarial pharmacokinetics;
  • History of hypersensitivity reactions or contraindications to any of the medicine(s) being tested or used as alternative treatments
  • Likehood of pre\-pubescence or pubescence in female.
  • Refusal to consent.
  • Not capable to comply with visit schedule.

Outcomes

Primary Outcomes

Not specified

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