Application of HBV Rapid Tests as a Tool for Wide-Use Screening (OPTISCREEN-B)
Is the Combination of Screening Algorithms and Use of Hepatitis B Rapid Tests Useful in Optimizing the Screening and Prevention of Hepatitis B?
With over 280 000 chronic carriers, 2,500 new annual cases and 1,300 deaths each year, hepatitis B is currently a frequent and potentially severe disease in France, despite efforts towards prevention and effective care.
In terms of prevention, France has very low immunization coverage (27.7%) and a high percentage of people ignoring HBV status (55%), leading to a delay in care. This is partly explained by poor knowledge of hepatitis B infection in the general population and an underestimation of the health impact of hepatitis B by doctors and health officials. Until recently, there have been no national guidelines governing its implementation (which is variable depending on the structures where screening is performed) and an insufficient evaluation of screening practices. Thus, data on the severity of liver disease, indications for treatment of HBV-infected patients and data on the use of vaccination for nonimmunized people are scarce. Furthermore, while HIV rapid tests are beginning to be used more widely, particularly to address the issue of people who do not come back and collect their results and to better adapt "counselling", their usefulness to detect of hepatitis B virus has not been evaluated to date.
The main objective of the Optiscreen B Study is to determine the benefit, if any, of using rapid tests as a screening tool to improve diagnosis, care and prevention of hepatitis B. Individuals risk of HBV-infection will be randomized into 2 groups, one group for which screening will be performed by usual serological test and a second group for which screening will be based on rapid tests. Centers will be selected to represent a diverse range of health centers whose aims include screening, prevention and/or vaccination.
研究概览
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
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Paris、法国、75003
- Centre de Santé au Maire-Volta
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Paris、法国、75012
- Centre d'examen de santé de la CPAM, antenne rue du Maroc
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Paris、法国、75012
- Consultation Policlinique de l'hôpital Saint-Antoine
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Paris、法国、75012
- Consultation Voyage de l'hôpital Saint-Antoine
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Paris、法国、75020
- CDAG de Belleville
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Born in a country of middle or high HBV endemicity
- Parents born in a country of middle or high HBV endemicity
- Travellers or residents from a country of middle or high HBV endemicity
- Blood, organ, tissue, sperm, and/or ovary donners or candidate donners.
- Health-care workers suspected of coming into direct contact with an HBV-infected individual and/or exposed to blood or any biological products from an HBV-infected individual
- Close contact with HBsAg-positive individuals (living in the same household, sexual partner, sharing needles, etc.)
- Individuals with accidental exposure to HBV
- Individuals with multiple sexual partners
- Men who have sex with men
- Pregnant women
- Hemodialysis
- Individuals requiring immunosuppressive therapy
- Individuals with persistently elevated transaminase levels
- HIV-positive
- Intravenous drug users
Exclusion Criteria:
- Age <18 years old
- Not capable of providing informed consent
- Already participated in a multi-center validation of HBV rapid tests
- Having, in their possession, irrefutable results of a prior test for hepatitis B virus
学习计划
研究是如何设计的?
设计细节
- 主要用途:放映
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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有源比较器:ELISA testing
HBV infection status determined by enzyme-linked immuno-assay (ELISA)
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Enzyme-linked immuno-assay (ELISA) will be used to determine hepatitis B surface antigen (HBsAg) and anti-HBsAg antibody (anti-HBs Ab) status.
Results will be given after test results are available (8-10 days).
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实验性的:Rapid testing
HBV infection status determined initially by a rapid test, then confirmed by enzyme-linked immuno-assay (ELISA).
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Enzyme-linked immuno-assay (ELISA) will be used to determine hepatitis B surface antigen (HBsAg) and anti-HBsAg antibody (anti-HBs Ab) status.
Results will be given after test results are available (8-10 days).
A rapid test will be performed to determine the subjects' hepatitis B surface antigen (HBsAg, using VIKIA®) and anti-HBs antibody status (anti-HBs Ab, using Quick ProfileTM).
Results will be given the same day.
其他名称:
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Percentage of Patients Appropriately Seeking Care
大体时间:6 months
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Subjects who are considered required to seek further care are as follows:
Of these patients, subjects who have achieved appropriate care are considered as follows:
The percentage of patients appropriately seeking care will be then calculated by the following formula: ((nb Vaccinated + nb infected with care) / (nb non-immunized + nb infected))*100 |
6 months
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合作者和调查者
调查人员
- 首席研究员:Julie Bottero, MD、Hôpital Saint-Antoine
出版物和有用的链接
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- IMEA 38
- 2011-A01603-38 (注册表标识符:ANSM)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
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