G6PD Deficiency, Malaria, Falciparum
Conditions
Keywords
Malaria, Falciparum, G6PD deficiency, Primaquine, Asia
Brief summary
In Cambodia, falciparum is becoming more difficult to treat because drugs are becoming less effective. The investigators can help to try to prevent the spread of this resistant malaria by adding a drug that will make it more difficult for the mosquito to drink up the malaria in people's blood. If the mosquito cannot drink up the malaria, then the malaria cannot develop in the mosquito so it will not be able to inject malaria back into people when it bites. The drug the investigators will use is called primaquine. Primaquine commonly causes the red cells in the blood to break apart if they are weak. Red cells need enzymes to work properly and weak red cells have low amounts of an enzyme called glucose 6 phosphate dehydrogenase (G6PD). The investigators want to know if treating malaria with primaquine will be safe for the red cells. To do this study, the investigators need to know if a subject has low G6PD or not.
Interventions
DRUGDihydroartemisinin piperaquine (DHA PP)
DRUGPrimaquine
Sponsors
National Centre for Parasitology, Entomology and Malaria Control, Cambodia
Institute Pasteur, Cambodia
World Health Organization
Centers for Disease Control and Prevention
Malaria Consortium
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
1 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age ≥ 1 year * Presentation with a confirmed fever (≥ 38⁰C axilla or ≥ 37.5⁰C aural) or history of fever in previous 48 hours +/- other clinical features of uncomplicated malaria * Plasmodium falciparum monoinfection ≥ 1 asexual form / 500 white blood cells * Informed consent (written/verbal) provided by patient or relative/legal guardian * Signed Assent form for children aged 12 to \< 18 years
Exclusion criteria
* Clinical signs of severe malaria or danger signs * Pregnant or breast feeding * Unable or unwilling to take a pregnancy test (for women of child-bearing age) * Women intending to become pregnant in the next 3 months * Allergic to primaquine or DHA PP * Patients taking drugs known to cause acute intravascular haemolytic anaemia (AIHA) in G6PD deficiency e.g. dapsone, nalidixic acid * Patients on treatment for a significant illness e.g. HIV, tuberculosis (TB) treatment, steroids * On drugs that could interfere with anti-malarial pharmacokinetics like antiretrovirals, cimetidine, ketoconazole, antiepileptic drugs, rifampicin
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Haemoglobin concentration | Day 7 | Compare haemoglobin concentrations in g/dL between the G6PD deficient arm given DHA PP plus primaquine, and the G6PD normal arm receiving the same regimen |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Piperaquine volume of distribution | Day 0-28 | Piperaquine apparent volume of distribution (Vd), modelled from population pharmacokinetic data from all patients receiving at least one dose of DHA PP +/- PQ |
| Peak plasma concentration (Cmax) of primaquine | Day 0-7 | Cmax taken directly from population pharmacokinetic data from all patients receiving at least one dose of DHA PP + PQ |
| Peak plasma concentration (Cmax) of piperaquine | Day 0-28 | Cmax taken directly from population pharmacokinetic data from all patients receiving at least one dose of DHA PP +/- PQ |
| Time to primquine peak plasma concentration (Tmax) | Day 0-7 | Tmax taken directly from population pharmacokinetic data from all patients receiving at least one dose of DHA PP + PQ |
| Time to piperaquine peak plasma concentration (Tmax) | Day 0-28 | Tmax taken directly from population pharmacokinetic data from all patients receiving at least one dose of DHA PP +/- PQ |
| Area under the plasma concentration versus time curve - primaquine | Day 0-7 | Modelled from population pharmacokinetic data from all patients receiving at least one dose of DHA PP + PQ |
| Area under the plasma concentration versus time curve - piperaquine | Day 0-28 | Modelled from population pharmacokinetic data from all patients receiving at least one dose of DHA PP +/- PQ |
| Determine G6PD enzyme activity | Day 0 | Quantitative G6PD testing among all participants using the G6PD enzyme assay from Trinity Biologicals, USA, yielding G6PD enzyme results in U/g Hb. |
| Assess usefulness of field adapted WHO haemoglobin colour card vs. Hemocue | Day 0 | Comparison of quantitative (HemoCue, g/dL HB) and qualitative (WHO haemolglobin colour card) estimates of haemoglobin concentration |
| Half life of piperaquine | Day 0-28 | Piperaquine terminal elimination half life, modelled from population pharmacokinetic data from all patients receiving at least one dose of DHA PP +/- PQ |
| Proportion patients with ≥25% change in haemoglobin as a marker of intravascular haemolysis | Change from Day 0 to Day 7 | Comparing across all 4 arms: proportion of all patients with fractional change in haemoglobin ≥25% from day 0 to day 7 |
| Plasma haemoglobin concentration as a marker of intravascular haemolysis | Day 7 | Comparing across all 4 arms: plasma haemoglobin concentration at day 7 |
| Urine colour change as a marker of intravascular haemolysis | Change from Day 0 to Day 7 | Change in urine colour grade from day 0 to day 7 (Hillmen, Hall et al. 2004) |
| Fractional change in haemoglobin as a marker of intravascular haemolysis | Change from Day 0 to Day 7 | Comparing across all 4 arms: fractional change in haemoglobin on day 7 vs. day 0 |
| Clearance rate of primaquine | Day 0-7 | Primaquine elimination clearance rate, modelled from population pharmacokinetic data from all patients receiving at least one dose of DHA PP + PQ |
| Half life of primaquine | Day 0-7 | Primaquine terminal elimination half life, modelled from population pharmacokinetic data from all patients receiving at least one dose of DHA PP + PQ |
| Primaquine volume of distribution | Day 0-7 | Primaquine apparent volume of distribution (Vd), modelled from population pharmacokinetic data from all patients receiving at least one dose of DHA PP + PQ |
| Clearance rate of piperaquine | Day 0-28 | Piperaquine elimination clearance rate, modelled from population pharmacokinetic data from all patients receiving at least one dose of DHA PP +/- PQ |
| Assess usefulness of rapid test for G6PDd in predicting acute intravascular haemolysis | Day 0 | Comparison of rapid G6PD test (AccessBio, USA) qualitative result against quantitative G6PD assay to determine predictive value for clinically significant haemolysis |
Countries
Cambodia
Outcome results
None listed