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Is there any evidence of antimalarial resistance to artemisinin derivatives in southern Laos?

Clinical investigation of in-vivo susceptibility of Plasmodium falciparum to artesunate in Xepon Inter-District Hospital, Savannakhet Province, Laos

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN12741594
Enrollment
40
Registered
2010-06-24
Start date
2010-06-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Plasmodium falciparum malaria, antimalarial drugs Infections and Infestations Plasmodium falciparum malaria

Interventions

Treatment arm 1: oral artesunate 2 mg/kg/day for 3 days followed by oral artemether-lumefantrine (20/120 mg): 1 dose twice daily for three days. Dosing by body weight will be: 1 tablet if less than 1

Sponsors

University of Oxford (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Male and female, aged greater than 10 years 2. Female patients between ages of 10 and 12 years old, provided they have not reached menarche, and those who have passed through the menopause 3. Mono-infection with P. falciparum as detected by microscopy 4. Parasitaemia of 10,000 - 175,000/µl asexual forms 5. Presence of axillary or tympanic temperature greater than or equal to 37.5°C or oral or rectal temperature of greater than or equal to 38°C or history of fever during the past 24 hours 6. Ability to swallow oral medication 7. Ability and willingness to comply with the study protocol for the duration of the study and to comply with the study visit schedule 8. Informed consent from the patient or from a parent or guardian in the case of children

Exclusion criteria

Exclusion criteria: 1. Presence of general danger signs or severe falciparum malaria according to the definitions of the World Health Organization (WHO, 2000) 2. Mixed or mono-infection with another Plasmodium species detected by microscopy 3. Presence of severe malnutrition (defined as a child whose growth standard is below -3 z-score, has symmetrical oedema involving at least the feet or has a mid-upper arm circumference less than 110 mm) 4. Presence of febrile conditions due to diseases other than malaria or other known underlying chronic or severe diseases 5. Regular medication, which may interfere with antimalarial pharmacokinetics 6. Received antimalarial drugs in the previous 48 hours 7. History of hypersensitivity reactions or contraindications to any of the medicine(s) used 8. Female patients of child-bearing age, defined as those who menstruate or are aged over 12 years and have not reached the menopause 9. Breastfeeding 10. Splenectomy

Design outcomes

Primary

MeasureTime frame
Number of patients with PCT greater than 72 hours. If six or more patients per treatment group (n = 20) have PCTs greater than 72 hours the trial will be stopped.

Secondary

MeasureTime frame
To assess the efficacy of artesunate 2 mg/kg/day and 4 mg/kg/day followed by 3-days artemether-lumefantrine in the treatment of uncomplicated P. falciparum malaria after 42-days follow up. Assessed on the basis of an assessment of the parasitological and clinical outcome of antimalarial treatment according to the latest WHO guidelines.

Countries

Laos

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026