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Effect of Liver and Blood-stage Treatment on Subsequent Plasmodium Reinfection and Morbidity

Primary Purpose

Plasmodium Vivax Infection, Plasmodium Vivax Clinical Episode, Plasmodium Falciparum Infection

Status
Completed
Phase
Phase 4
Locations
Papua New Guinea
Study Type
Interventional
Intervention
Primaquine
Placebo
Chloroquine
Artemether Lumefantrine
Sponsored by
Papua New Guinea Institute of Medical Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Plasmodium Vivax Infection focused on measuring Plasmodium vivax, Hypnozoites, Primaquine, Liver-stage, Blood-stage, Plasmodium falciparum

Eligibility Criteria

5 Years - 10 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • aged 5-10 years (±3 months)
  • permanent residents of the area
  • absence of history of hypersensitivity reactions to the drugs

Exclusion Criteria:

  • chronic illness
  • severe malnutrition (weight-for-age nutritional Z score [WAZ] <60th percentile)
  • severe anemia (Hb <5 g/dL),
  • G-6-PD deficiency (<60% G-6-PD activity)
  • permanent disability, which prevents or impedes study participation. Any 1 or more of the criteria is sufficient to exclude study participation.

Sites / Locations

  • PNG Institute of Medical Research

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Primaquine

Placebo

Arm Description

Primaquine, 0.5mg/kg/day, 20 days directly observed treatment Chloroquine, 25mg/kg total dose, divided over 3 days directly observed treatment Artemether-Lumefantrine, 3 days BD

Placebo, 20 days directly observed treatment Chloroquine, mg/kg, 3 days directly observed treatment Artemether-Lumefantrine, 3 days BD

Outcomes

Primary Outcome Measures

Time to first or only Plasmodium vivax infection by light microscopy and PCR
Time to first or only clinical P. vivax episode

Secondary Outcome Measures

Time to first or only P. falciparum infection by light microscopy and PCR
Time to first or only P. ovale infection by light microscopy and PCR
Time to first or only P. malariae infection by light microscopy and PCR

Full Information

First Posted
May 19, 2014
Last Updated
May 19, 2014
Sponsor
Papua New Guinea Institute of Medical Research
Collaborators
Walter and Eliza Hall Institute of Medical Research, Swiss Tropical & Public Health Institute, Barcelona Centre for International Health Research
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1. Study Identification

Unique Protocol Identification Number
NCT02143934
Brief Title
Effect of Liver and Blood-stage Treatment on Subsequent Plasmodium Reinfection and Morbidity
Official Title
Host and Parasites Factors Contributing to Risk of Plasmodium Re-infection and Morbidity in Elementary School Children in Maprik, East Sepik Province
Study Type
Interventional

2. Study Status

Record Verification Date
May 2014
Overall Recruitment Status
Completed
Study Start Date
August 2009 (undefined)
Primary Completion Date
May 2010 (Actual)
Study Completion Date
May 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Papua New Guinea Institute of Medical Research
Collaborators
Walter and Eliza Hall Institute of Medical Research, Swiss Tropical & Public Health Institute, Barcelona Centre for International Health Research

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study specifically seeks to quantify the contribution of relapes to the burden of P. vivax infections and disease by determining on the effect of radical pre-erythrocytic and erythrocytic clearance on subsequent rates of Plasmodium spp. infection and disease in children aged 5-10 years in a treatment to re-infection study design. In order the clear liver-stage/blood-stages G6PD-normal children were randomised to receive Chloroquine (3 days, standard dose) and Coartem (3 days, standard dose) plus either i) primaquine (20 days, 0.5mg/kg) or ii) placebo (20days). These drugs were administered over a period of 4 weeks. In addition to this epidemiological data, the study will assess the natural acquisition of cellular and humoral immune responses to P. falciparum and P. vivax, thus assisting in the determination of correlates of clinical immunity to P. falciparum and P. vivax in PNG children aged 5-10 years. These data will not only be essential for development of future vaccines against P. vivax and P falciparum but provide invaluable insight into the contribution of long-lasting liver-stages to the force of infection with P. vivax that will contribute towards designing more rational approaches to the treatment of P. vivax both in the context of case management and future attempts at elimination.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Plasmodium Vivax Infection, Plasmodium Vivax Clinical Episode, Plasmodium Falciparum Infection, Plasmodium Falciparum Clinical Episode
Keywords
Plasmodium vivax, Hypnozoites, Primaquine, Liver-stage, Blood-stage, Plasmodium falciparum

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
524 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Primaquine
Arm Type
Active Comparator
Arm Description
Primaquine, 0.5mg/kg/day, 20 days directly observed treatment Chloroquine, 25mg/kg total dose, divided over 3 days directly observed treatment Artemether-Lumefantrine, 3 days BD
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo, 20 days directly observed treatment Chloroquine, mg/kg, 3 days directly observed treatment Artemether-Lumefantrine, 3 days BD
Intervention Type
Drug
Intervention Name(s)
Primaquine
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Sugar pills, appearance identical to Primaquine tablets
Intervention Type
Drug
Intervention Name(s)
Chloroquine
Intervention Type
Drug
Intervention Name(s)
Artemether Lumefantrine
Other Intervention Name(s)
Coartem
Primary Outcome Measure Information:
Title
Time to first or only Plasmodium vivax infection by light microscopy and PCR
Time Frame
8 months post-baseline
Title
Time to first or only clinical P. vivax episode
Time Frame
8 months post-baseline
Secondary Outcome Measure Information:
Title
Time to first or only P. falciparum infection by light microscopy and PCR
Time Frame
8 months post-baseline
Title
Time to first or only P. ovale infection by light microscopy and PCR
Time Frame
8 months post-baseline
Title
Time to first or only P. malariae infection by light microscopy and PCR
Time Frame
8 months post-baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: aged 5-10 years (±3 months) permanent residents of the area absence of history of hypersensitivity reactions to the drugs Exclusion Criteria: chronic illness severe malnutrition (weight-for-age nutritional Z score [WAZ] <60th percentile) severe anemia (Hb <5 g/dL), G-6-PD deficiency (<60% G-6-PD activity) permanent disability, which prevents or impedes study participation. Any 1 or more of the criteria is sufficient to exclude study participation.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ivo Mueller, PhD
Organizational Affiliation
Walter and Eliza Hall Institute of Medical Research; Centre de Recerca en Salut Internacional de Barcelona (CRESIB)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Inoni Betuela, MD PhD
Organizational Affiliation
PNG Institute of Medical Research
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Louis Schofield, PhD
Organizational Affiliation
Walter and Eliza Hall Institute of Medical Research
Official's Role
Principal Investigator
Facility Information:
Facility Name
PNG Institute of Medical Research
City
Maprik
State/Province
East Sepik Province
Country
Papua New Guinea

12. IPD Sharing Statement

Citations:
PubMed Identifier
36099312
Citation
Holzschuh A, Gruenberg M, Hofmann NE, Wampfler R, Kiniboro B, Robinson LJ, Mueller I, Felger I, White MT. Co-infection of the four major Plasmodium species: Effects on densities and gametocyte carriage. PLoS Negl Trop Dis. 2022 Sep 13;16(9):e0010760. doi: 10.1371/journal.pntd.0010760. eCollection 2022 Sep.
Results Reference
derived
PubMed Identifier
28862132
Citation
Hofmann NE, Karl S, Wampfler R, Kiniboro B, Teliki A, Iga J, Waltmann A, Betuela I, Felger I, Robinson LJ, Mueller I. The complex relationship of exposure to new Plasmodium infections and incidence of clinical malaria in Papua New Guinea. Elife. 2017 Sep 1;6:e23708. doi: 10.7554/eLife.23708.
Results Reference
derived
PubMed Identifier
28732068
Citation
Wampfler R, Hofmann NE, Karl S, Betuela I, Kinboro B, Lorry L, Silkey M, Robinson LJ, Mueller I, Felger I. Effects of liver-stage clearance by Primaquine on gametocyte carriage of Plasmodium vivax and P. falciparum. PLoS Negl Trop Dis. 2017 Jul 21;11(7):e0005753. doi: 10.1371/journal.pntd.0005753. eCollection 2017 Jul.
Results Reference
derived
PubMed Identifier
26505753
Citation
Robinson LJ, Wampfler R, Betuela I, Karl S, White MT, Li Wai Suen CS, Hofmann NE, Kinboro B, Waltmann A, Brewster J, Lorry L, Tarongka N, Samol L, Silkey M, Bassat Q, Siba PM, Schofield L, Felger I, Mueller I. Strategies for understanding and reducing the Plasmodium vivax and Plasmodium ovale hypnozoite reservoir in Papua New Guinean children: a randomised placebo-controlled trial and mathematical model. PLoS Med. 2015 Oct 27;12(10):e1001891. doi: 10.1371/journal.pmed.1001891. eCollection 2015 Oct.
Results Reference
derived

Learn more about this trial

Effect of Liver and Blood-stage Treatment on Subsequent Plasmodium Reinfection and Morbidity

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