search
Back to results

Neonatal Vaccination Against Hepatitis B in Africa - Sero-survey in Senegal (NeoVac2S)

Primary Purpose

Hepatitis B

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Human biological samples
Sponsored by
Institut Pasteur
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Hepatitis B

Eligibility Criteria

9 Months - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

All mothers of children between 9 and 12 months of age registered in the SSDS of Niakhar, Bambey and Fatick, who accept a blood sample from her and their child.

Exclusion Criteria:

  • A child without a mother identified for sampling
  • Failure to sign informed consent to participate in the NeoVac 2 study

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Children and their mothers

    Arm Description

    Human biological samples from children aged 9 to 12 months and their mothers. Capillary and venous blood samples.

    Outcomes

    Primary Outcome Measures

    Vaccination coverage of the vaccine at birth from the health record and health post registers
    Collection of thedate of vaccination of children aged 9-12 months

    Secondary Outcome Measures

    Positive HBsAg among mothers of children aged 9-12 months
    HBsAg testing from capillary blood on site
    Positive HBsAg among children aged 9-12 months
    HBsAg testing from capillary blood on site

    Full Information

    First Posted
    February 1, 2019
    Last Updated
    March 8, 2022
    Sponsor
    Institut Pasteur
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT03829735
    Brief Title
    Neonatal Vaccination Against Hepatitis B in Africa - Sero-survey in Senegal
    Acronym
    NeoVac2S
    Official Title
    Neonatal Vaccination Against Hepatitis B in Africa - Sero-survey in Senegal
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2022
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Not started
    Study Start Date
    November 1, 2020 (Anticipated)
    Primary Completion Date
    June 30, 2021 (Actual)
    Study Completion Date
    August 30, 2021 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Institut Pasteur

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Chronic infection with hepatitis B virus (HBV) is a leading cause of death in adults in sub-Saharan Africa (SSA). Prior to the introduction of the hepatitis B vaccine, main modes of transmission in SSA were perinatal transmission from mother-to-child (MTCT) (10%) and horizontal transmission during early childhood (90%). MTCT occurs through contact with maternal fluids during passage through the birth cana; transplacental transmission and transmission through breastfeeding are rare. In 2009, WHO recommended the administration of hepatitis B vaccination to all newborns within 24 hours of birth to prevent perinatal and early transmissions. In Senegal, the government introduced the monovalent vaccine that can be used within 24 hours after birth in the Expanded Program on Immunization (EPI) in March 2016. Here, we present a study protocol for a sero-epidemiological study of pairs of children aged 9 to 12 months and their mothers, identified through the demographic study, to assess the impact of monovalent vaccine introduced by the national program for prevention of mother-to-child transmission in Senegal. We will also assess the diagnostic performance of loop-mediated isothermal amplification assay (LAMP) to identify people with high viral replication (HBV DNA ≥200,000 IU/ml), compared to a conventional reference test (PCR).
    Detailed Description
    Chronic infection with hepatitis B virus (HBV) is a leading cause of death in adults in sub-Saharan Africa (SSA). Each year, about 61,000 people are estimated to die of hepatocellular carcinoma (HCC) or cirrhosis secondary to chronic infection with HBV. Prior to the introduction of the hepatitis B vaccine, main modes of transmission in SSA were perinatal transmission from mother-to-child (MTCT) (10%) and horizontal transmission during early childhood (90%). MTCT occurs through contact with maternal fluids during passage through the birth cana; transplacental transmission and transmission through breastfeeding are rare. Despite a relatively low frequency of perinatal transmission in SSA, prevention of this type of transmission is important, because this mode of transmission results in higher risk of becoming chronic HBV carriers, and developing chronic liver disease, including HCC, than horizontal transmission. In 2009, WHO recommended the administration of hepatitis B vaccination to all newborns within 24 hours of birth to prevent perinatal and early transmissions. In Senegal, the government introduced the monovalent vaccine that can be used within 24 hours after birth in the Expanded Program on Immunization (EPI) in March 2016. It is in this context that the NeoVac study started in 2016 in Senegal, Burkina Faso and Madagascar. The general objective is to develop a long-term strategy adapted to the local context to vaccinate newborns against hepatitis B in the first 24 hours of life. The NeoVac 1, a population-based epidemiological survey to estimate the coverage of this newly introduced monovalent hepatitis B vaccine started in Senegal in 2018. Here, we present a study protocol for a sero-epidemiological study of pairs of children aged 9 to 12 months and their mothers, identified through the demographic study, to assess the impact of monovalent vaccine introduced by the national program for prevention of mother-to-child transmission in Senegal. We will also assess the diagnostic performance of loop-mediated isothermal amplification assay (LAMP) to identify people with high viral replication (HBV DNA ≥200,000 IU/ml), compared to a conventional reference test (PCR).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Hepatitis B

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Children and their mothers
    Arm Type
    Experimental
    Arm Description
    Human biological samples from children aged 9 to 12 months and their mothers. Capillary and venous blood samples.
    Intervention Type
    Other
    Intervention Name(s)
    Human biological samples
    Intervention Description
    Collection of capillary blood for HbsAg testing. Collection of 12 mL of blood for HbsAg positive women and 1 mL for HbsAg positive children.
    Primary Outcome Measure Information:
    Title
    Vaccination coverage of the vaccine at birth from the health record and health post registers
    Description
    Collection of thedate of vaccination of children aged 9-12 months
    Time Frame
    9 to 12 months post-natal visit
    Secondary Outcome Measure Information:
    Title
    Positive HBsAg among mothers of children aged 9-12 months
    Description
    HBsAg testing from capillary blood on site
    Time Frame
    9 to 12 months post-natal visit
    Title
    Positive HBsAg among children aged 9-12 months
    Description
    HBsAg testing from capillary blood on site
    Time Frame
    9 to 12 months post-natal visit

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    9 Months
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: All mothers of children between 9 and 12 months of age registered in the SSDS of Niakhar, Bambey and Fatick, who accept a blood sample from her and their child. Exclusion Criteria: A child without a mother identified for sampling Failure to sign informed consent to participate in the NeoVac 2 study
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Fabien Taieb
    Organizational Affiliation
    Institut Pasteur Dakar
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Neonatal Vaccination Against Hepatitis B in Africa - Sero-survey in Senegal

    We'll reach out to this number within 24 hrs