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临床试验/NCT01412567
NCT01412567已完成不适用

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

Govind Ballabh Pant Hospital1 个研究点 分布在 1 个国家目标入组 259 人开始时间: 2005年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
259
试验地点
1
主要终点
remaining free of any HBV infection (either overt or occult) plus development of adequate immune response to vaccine at 18 weeks of age

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Prevention
盲法
Double (Participant, Investigator)

入排标准

年龄范围
— 至 1 Day(Child)
性别
All
接受健康志愿者

入选标准

  • Newborn babies of mothers who were found to be HBsAg positive

排除标准

  • 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.

研究组 & 干预措施

Vaccine+HBIG

Active Comparator

干预措施: Vaccine+HBIG (Drug)

Vaccine+Placebo

Placebo Comparator

干预措施: Vaccine+Placebo (Drug)

结局指标

主要结局

remaining free of any HBV infection (either overt or occult) plus development of adequate immune response to vaccine at 18 weeks of age

时间窗: 18 weeks

次要结局

未报告次要终点

研究者

申办方类型
Other Gov

研究点 (1)

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