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Withdrawn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
About this trial
This is an interventional diagnostic trial for Hepatitis B
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
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
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Withdrawn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
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