Vaccine+HBIG Versus Vaccine+Placebo for Newborns of HBsAg+ Mothers
Primary Purpose
Chronic Hepatitis B
Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Vaccine+HBIG
Vaccine+Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Chronic Hepatitis B focused on measuring Hepatitis B, HBsAg, Antenatal, Pregnancy, Vertical transmission, Placenta, HBV DNA
Eligibility Criteria
Inclusion Criteria:
- Newborn babies of mothers who were found to be HBsAg positive
Exclusion Criteria:
- Babies of mothers who had any symptoms of liver disease during the pregnancy such as jaundice, pruritus, ascites, or gastrointestinal bleed;
- Babies of mothers taking anti-viral treatment during pregnancy;
- Babies of mother with pregnancy related complications; and
- Babies of mothers who refused to participate in the study.
Sites / Locations
- Lady Hardinge Medical College
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Vaccine+HBIG
Vaccine+Placebo
Arm Description
Outcomes
Primary Outcome Measures
remaining free of any HBV infection (either overt or occult) plus development of adequate immune response to vaccine at 18 weeks of age
Secondary Outcome Measures
Full Information
NCT ID
NCT01412567
First Posted
August 8, 2011
Last Updated
August 8, 2011
Sponsor
Govind Ballabh Pant Hospital
Collaborators
Indian Council of Medical Research, Lady Hardinge Medical College
1. Study Identification
Unique Protocol Identification Number
NCT01412567
Brief Title
Vaccine+HBIG Versus Vaccine+Placebo for Newborns of HBsAg+ Mothers
Official Title
Comparison of Recombinant Hepatitis B Vaccine Plus Hepatitis B Immune Globulin (HBIG) Versus Vaccine Plus Placebo for Prophylaxis of Hepatitis B Infection in Newborns of Hepatitis B Surface Antigen (HBsAg) Positive Mothers
Study Type
Interventional
2. Study Status
Record Verification Date
August 2011
Overall Recruitment Status
Completed
Study Start Date
October 2005 (undefined)
Primary Completion Date
June 2010 (Actual)
Study Completion Date
June 2010 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Govind Ballabh Pant Hospital
Collaborators
Indian Council of Medical Research, Lady Hardinge Medical College
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Prevention of perinatal transmission is essential to decrease the global burden of chronic HBV. Recombinant HBV vaccine and hepatitis B immunoglobulin (HBIG) given after delivery to the newborns of HBsAg positive mothers is the standard of care for prevention of HBV in babies. Some studies have however, shown that vaccine alone may be equally effective. Hence, immunoprophylaxis with hepatitis B vaccine with or without HBIG is effective in prevention of transmission of overt HBV infection to the babies. The primary outcome measure of most of the trials on immunoprophylaxis was the occurrence of hepatitis B, defined as a blood specimen positive for hepatitis B surface antigen (HBsAg). However, whether this immunoprophylaxis also prevents HBsAg negative HBV infection (occult HBV infection) in babies is not known. In the present study the investigators evaluated the efficacy of the two regimens; vaccination alone and compared it with vaccination plus HBIG administration at birth in preventing transmission of both overt and occult HBV infection to the newborn babies.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Hepatitis B
Keywords
Hepatitis B, HBsAg, Antenatal, Pregnancy, Vertical transmission, Placenta, HBV DNA
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
259 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Vaccine+HBIG
Arm Type
Active Comparator
Arm Title
Vaccine+Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Vaccine+HBIG
Intervention Description
Recombinant hepatitis B vaccine at birth, 6 weeks, 10 weeks, and 14 weeks in the dose of 10 mcg (0.5 mL), by intramuscular injection in the anterolateral thigh; PLUS HBIG in the dose of 0.5 mL intramuscularly immediately after birth
Intervention Type
Drug
Intervention Name(s)
Vaccine+Placebo
Intervention Description
Recombinant hepatitis B vaccine at birth, 6 weeks, 10 weeks, and 14 weeks in the dose of 10 mcg (0.5 mL), by intramuscular injection in the anterolateral thigh; PLUS placebo intramuscularly immediately after birth
Primary Outcome Measure Information:
Title
remaining free of any HBV infection (either overt or occult) plus development of adequate immune response to vaccine at 18 weeks of age
Time Frame
18 weeks
10. Eligibility
Sex
All
Maximum Age & Unit of Time
1 Day
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Newborn babies of mothers who were found to be HBsAg positive
Exclusion Criteria:
Babies of mothers who had any symptoms of liver disease during the pregnancy such as jaundice, pruritus, ascites, or gastrointestinal bleed;
Babies of mothers taking anti-viral treatment during pregnancy;
Babies of mother with pregnancy related complications; and
Babies of mothers who refused to participate in the study.
Facility Information:
Facility Name
Lady Hardinge Medical College
City
New Delhi
State/Province
Delhi
ZIP/Postal Code
110001
Country
India
12. IPD Sharing Statement
Citations:
PubMed Identifier
24168259
Citation
Pande C, Sarin SK, Patra S, Kumar A, Mishra S, Srivastava S, Bhutia K, Gupta E, Mukhopadhyay CK, Dutta AK, Trivedi SS. Hepatitis B vaccination with or without hepatitis B immunoglobulin at birth to babies born of HBsAg-positive mothers prevents overt HBV transmission but may not prevent occult HBV infection in babies: a randomized controlled trial. J Viral Hepat. 2013 Nov;20(11):801-10. doi: 10.1111/jvh.12102. Epub 2013 Apr 23.
Results Reference
derived
Learn more about this trial
Vaccine+HBIG Versus Vaccine+Placebo for Newborns of HBsAg+ Mothers
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