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Prevention of P. Vivax Malaria During Pregnancy in Bolivia

Primary Purpose

Malaria

Status
Withdrawn
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Chloroquine profilaxis
Sponsored by
Institut de Recherche pour le Developpement
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Malaria focused on measuring malaria, Plasmodium vivax, pregnancy, chemoprophylaxis

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Pregnancy between 4 to 36 weeks of gestation Intention to deliver at the maternity clinics Residence near the maternity clinics Written informed consent (parents or tutors if aged<18 years) Exclusion Criteria: Pregnancy prior to 4 weeks or after 36 weeks of gestation Allergy to chloroquine Clinical signs of hepatic or renal alteration Inability to take drugs by oral route Presence of effective uterine contractions

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Chloroquine profilaxis

    No prevention

    Arm Description

    Prevention: chloroquine profilaxis Prevention of malaria attacks with chloroquine profilaxis taken once a week

    Treatment of malaria attack with chloroquine when they occur

    Outcomes

    Primary Outcome Measures

    Incidence of women presenting a malaria attack during pregnancy

    Secondary Outcome Measures

    proportions of mothers with placental plasmodial infection
    proportions of mothers with moderate to severe anaemia (<8g/dl) at delivery
    maternal haemoglobin rate at delivery
    proportions of women with parasitaemia during pregnancy and at delivery
    mean parasites densities of women with parasitaemia during pregnancy and at delivery
    proportions of children with low birthweight (<2,500 grams)
    mean birthweight
    proportions of preterm deliveries

    Full Information

    First Posted
    February 9, 2006
    Last Updated
    May 21, 2013
    Sponsor
    Institut de Recherche pour le Developpement
    Collaborators
    Instituto Nacional de Laboratorios de Salud (INLASA), Pan American Health Organization, Ministry of Health, Bolivia
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00290420
    Brief Title
    Prevention of P. Vivax Malaria During Pregnancy in Bolivia
    Official Title
    Prevention of P. Vivax Malaria During Pregnancy: Effects on Mother and Child Health in Santa Cruz, Bolivia. Open, Multicentric, Randomized Clinical Trial, Comparing Prophylaxis Once a Week to Malaria Attack Treatment, Both by Chloroquine.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2013
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    important delays and malaria season missed, due to political changes
    Study Start Date
    March 2006 (undefined)
    Primary Completion Date
    November 2007 (Anticipated)
    Study Completion Date
    November 2007 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Institut de Recherche pour le Developpement
    Collaborators
    Instituto Nacional de Laboratorios de Salud (INLASA), Pan American Health Organization, Ministry of Health, Bolivia

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of this study is to determine which, between weekly prophylaxis or malaria attack treatment, both by chloroquine, is the most appropriate way to protect women and foetus from P. vivax malaria infection during pregnancy.
    Detailed Description
    It has been demonstrated that malaria is responsible for anaemia during pregnancy and reduces birth weight among newborns. In Bolivia, malaria is mostly caused by P. vivax. Maternal and foetal consequences of P. vivax infections have been poorly investigated until now, over all in South America. In fact, recommendations for the protection of pregnant women from malaria in Bolivia have not been clearly established. Prophylaxis by chloroquine is still recommended in other continents than Africa, mainly because chloroquine resistances are still uncommon in P. vivax species. The alternative way to protect women during pregnancy is to treat malaria attacks during antenatal visits. For this purpose, we will realize a study in order to assess the most appropriate way to protect women and foetus from malaria infection, i.e. weekly prophylaxis or mild malaria attack treatment, both by chloroquine. By realizing a randomized and multicentric clinical trial on 800 women in each group, we will compare the impact on maternal malaria attack incidence rates, on proportions of mothers with anaemia, on low-birth weight and on positive parasitaemias during pregnancy and at delivery, of weekly prophylaxis and mild malaria attack diagnosis and treatment. The study will be undertaken during 18 months in the region of Santa Cruz and will give important information to the Bolivian Ministry of Health for establishing national recommendations.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Malaria
    Keywords
    malaria, Plasmodium vivax, pregnancy, chemoprophylaxis

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Chloroquine profilaxis
    Arm Type
    Experimental
    Arm Description
    Prevention: chloroquine profilaxis Prevention of malaria attacks with chloroquine profilaxis taken once a week
    Arm Title
    No prevention
    Arm Type
    No Intervention
    Arm Description
    Treatment of malaria attack with chloroquine when they occur
    Intervention Type
    Drug
    Intervention Name(s)
    Chloroquine profilaxis
    Other Intervention Name(s)
    prevention of plasmodium vivax malaria harmfull effects on birth outcomes
    Intervention Description
    Prevention: Give a profilaxis with chloroquine once a week to prevent Plasmodium vivax malaria attacks and to prevent harmfull effect on birth outcomes
    Primary Outcome Measure Information:
    Title
    Incidence of women presenting a malaria attack during pregnancy
    Time Frame
    two years
    Secondary Outcome Measure Information:
    Title
    proportions of mothers with placental plasmodial infection
    Time Frame
    2 years
    Title
    proportions of mothers with moderate to severe anaemia (<8g/dl) at delivery
    Time Frame
    2 years
    Title
    maternal haemoglobin rate at delivery
    Time Frame
    2 years
    Title
    proportions of women with parasitaemia during pregnancy and at delivery
    Time Frame
    2 years
    Title
    mean parasites densities of women with parasitaemia during pregnancy and at delivery
    Time Frame
    2 years
    Title
    proportions of children with low birthweight (<2,500 grams)
    Time Frame
    2 years
    Title
    mean birthweight
    Time Frame
    2 years
    Title
    proportions of preterm deliveries
    Time Frame
    2 years

    10. Eligibility

    Sex
    Female
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Pregnancy between 4 to 36 weeks of gestation Intention to deliver at the maternity clinics Residence near the maternity clinics Written informed consent (parents or tutors if aged<18 years) Exclusion Criteria: Pregnancy prior to 4 weeks or after 36 weeks of gestation Allergy to chloroquine Clinical signs of hepatic or renal alteration Inability to take drugs by oral route Presence of effective uterine contractions
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Michel Cot, MD-PhD
    Organizational Affiliation
    Institut de Recherche pour le Developpement
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Laurent Brutus, MD-MSc
    Organizational Affiliation
    Institut de Recherche pour le Développement, IRD, Bolivia
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Agnès Le Port, MSc
    Organizational Affiliation
    Institut de Recherche pour le Développement, IRD, Bolivia
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Prevention of P. Vivax Malaria During Pregnancy in Bolivia

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