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Completed

NCT Number: NCT01935882

Low Dose Primaquine for Clearance of Gametocytes

Primaquine (PQ) is currently the only available drug that can clear mature transmission stages of P. falciparum parasites. PQ was previously shown to clear gametocytes that persist after artemisinin-combination therapy. However, there are safety concerns about the use of PQ at the currently recommended dose of 0.75mg/kg in individuals who are glucose-6-phosphate dehydrogenase (G6PD) deficient. PQ causes transient but significant haemolysis in G6PD deficient individuals; this side-effect is dose dependent. There are indications that a lower dosing of PQ may effectively reduce gametocyte carriage but the lowest efficacious dose for gametocyte clearance is currently unknown. Recently, the World Health Organization changed their recommendation to a low dose of primaquine, 0.25mg/kg. However, there is no direct evidence on the extent to which (low dose) PQ prevents malaria transmission to mosquitoes and what the lowest efficacious dose is.

In the current study we aim to identify the lowest efficacious dose of PQ in individuals with normal G6PD function. Children with asymptomatic malaria and normal G6PD enzyme function will be randomized to treatment with artemether-lumefantrine alone or in combination with low doses of PQ. All enrolled individuals will receive a full three-day course of AL, and will be randomized to receive a dose of primaquine or placebo with their fifth dose of AL. Efficacy will be determined based on gametocyte carriage during follow-up, measured by molecular methods. For a subset of participants with patent gametocytes, primaquine effect on infectivity to mosquitoes will be assessed by membrane feeding assays

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Key information

Age range

2 year–15 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Centre National de Recherche et de Formation sur le Paludisme

Ouagadougou, Burkina Faso

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age > 2 years and <15 years
  • Weight over 10kg
  • P. falciparum parasitaemia >1,000 parasites and <200,000 parasites/µl
  • P. falciparum gametocytes detected by microscopy
  • Normal G6PD enzyme function
  • Informed consent by legally acceptable representative

Exclusion criteria

  • Enrolled in another study
  • Fever or history of fever in the last 24 hours
  • Evidence of severe illness/ danger signs
  • Known allergy to study medications
  • Hb < 8g/dL
  • Started menstruation
  • Pregnancy or breastfeeding
  • Antimalarials taken within the last 2 days
  • Primaquine taken within the last 4 weeks
  • Blood transfusion within the last 90 days
  • Non-falciparum malaria co-infection

Treatment and study plan

Artemether-lumefantrine combination

Drug

Artemether-Lumefantrine with a single dose of 0.25mg/kg primaquine

Drug

Artemether-Lumefantrine with a single dose of 0.4mg/kg primaquine

Drug

Primary outcomes

  1. Gametocyte carriage

    Time frame: 14 days during follow-up

    Gametocyte prevalence at enrolment and on days 2, 3, 7, 10, 14 during follow-up.

    The duration of gametocyte carriage in days will be estimated.

Secondary outcomes

  1. Transmission to Anopheles gambiae mosquitoes

    Time frame: day -1, day 3, day 7

    Mosquito membrane feeding assays will be used to determine the proportion of infected mosquitoes and the oocyst burden in infected mosquitoes.

  2. Haematological recovery

    Time frame: 14 days during follow-up

    Haemoglobin concentration will be determined at enrolment and on days 2, 3, 7, 10 and 14 during follow-up. Haemoglobin concentration will be presented as grams per decilitre and as concentration relative to enrolment value.

  3. Primaquine and lumefantrine pharmacokinetics

    Time frame: 7 days during follow-up

    The pharmacokinetic sampling will measure primaquine, lumefantrine and metabolites. Sampling involves 7 venous blood samples during the first 72 hours after treatment and a single later time point at day 7 post initiation of treatment. Drug plasma levels will be related to treatment arm and to the participant's Cytochrome P450 2D6 metabolizer status. CYP2D6 is an enzyme involved in primaquine metabolism.

Sponsors and collaborators

Lead sponsor

London School of Hygiene and Tropical Medicine

Other

Collaborators

  • Centre national de recherche et de formation sur le paludisme
  • Radboud University Medical Center

Registry information

Official study title

A Double Blind Randomized Controlled Trial to Assess the Efficacy and Safety of Low Dose Primaquine for Clearance of Gametocytes in Asymptomatic Individuals Infected With P. Falciparum in Burkina Faso

Acronym: LOPRIM

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
Sep 5, 2013
Registry last updated
Sep 2, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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