Skip to main content
OpenTrials
Completed

NCT Number: NCT02389374

A Study to Assess Safety of Current Standard Malaria Treatment and an Assessment of G6PD Status in South-east Bangladesh

This is a study assessing safety and efficacy of current national guidelines for the treatment of uncomplicated malaria in Bangladesh as well as to assess the G6PD status among the enrolled patients.

Completed

Looking for future studies?

Notify Me

Key information

Age range

12 month and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

About this study

The national guidelines for the treatment of uncomplicated malaria in Bangladesh currently recommend a standard dose of artemether-lumefantrine followed by a single dose of primaquine for P. falciparum malaria and a three day course of chloroquine followed by 14 days of primaquine for vivax malaria.Currently the national treatment guidelines do not include any testing for G6PD deficiency before treatment with primaquine. In order to guarantee safe and efficacious treatment for all patients diagnosed with uncomplicated malaria in Bangladesh, it is essential to monitor the effectiveness and safety of the recommended treatment guidelines. This trial therefore evaluates the local efficacy and safety of the current first line treatment and assesses the G6PD status of the enrolled patients.

Patients with uncomplicated malaria attending the health care center, who meet the study inclusion criteria will be enrolled, treated on site and followed up for 28 days. The follow-up will consist of a fixed schedule of check-up visits and corresponding clinical and laboratory examinations. The study will provide efficacy data for both artemether-lumefantrine and chloroquine and will generate data on G6PD status in the region, which will provide vital information for policy makers in regards to the wider roll out of primaquine for the radical cure of vivax malaria.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥ 12 months
  • P. vivax or P. falciparum monoinfection or P.v. / P.f. mixed infection
  • Presence of axillary temperature ≥ 37.5°C or history of fever during the past 24 hrs
  • Ability to swallow oral medication.
  • Ability and willingness to comply with the study protocol for the duration of the study
  • Informed consent/assent from the patient or from a parent or guardian in the case of children.

Exclusion criteria

  • Presence of general danger signs in children aged under 5 years or signs of severe malaria according to the definitions of WHO
  • Presence of severe malnutrition
  • Acute anaemia <8g/dL
  • Regular medication, which may interfere with antimalarial pharmacokinetics
  • History of hypersensitivity reactions or contraindications to any of the drug(s) tested or used as alternative treatment(s)
  • A positive pregnancy test or lactating

Treatment and study plan

Chloroquine

Drug

standard dose

Artemether-lumefantrine combination

Drug

standard dose

Primaquine

Drug

single dose

Primary outcomes

  1. The Proportion of Adverse and Serious Adverse Events Following Unsupervised Primaquine Treatment

    Time frame: during follow up (day 28)

    The proportion of adverse and serious adverse events following unsupervised primaquine treatment until day 28

Secondary outcomes

  1. Proportion of Patients Receiving Blood Transfusion and With Severe Anaemia (Hb<7g/dl)

    Time frame: day 28

  2. Fractional Change in Hb Between Baseline and Day 9 and 16

    Time frame: day 0 and 16

  3. Proportion of Patients With Anaemia Less Than 8g/dl on Day 2

    Time frame: on day 2

  4. Proportion of Patients With Any Parasitemia on Day 3 After Treatment

    Time frame: day 3

  5. Proportion of Patients With Fever on Day 2 After Treatment

    Time frame: day 2

  6. Recurrence of Parasitaemia Within 16 Days of Follow up

    Time frame: day 16

  7. Proportion of Patients Adhering to 14 Days of Primaquine Treatment in the Vivax Cohort as Measured by Pill Count

    Time frame: day 16

  8. The Distribution of G6PD Activity Measured in U/gHb Among All Malaria Patients

    Time frame: day 0

  9. Frequency and Type of Variants of the G6PD Gene Within the Study Population

    Time frame: day 0 or 1

    Frequency and type of variants of the G6PD gene within the study population

Sponsors and collaborators

Lead sponsor

Menzies School of Health Research

Other

Collaborators

  • International Centre for Diarrhoeal Disease Research, Bangladesh

Registry information

Official study title

A Study to Assess Safety of Current Standard Malaria Treatment and an Assessment of Glucose-6-dehydrogenase Status in South-east Bangladesh

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Mar 17, 2015
Registry last updated
Mar 13, 2024

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.

Published trials that share one or more normalized conditions with this study.