- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT01767597
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.
연구 개요
연구 유형
등록 (실제)
단계
- 해당 없음
연락처 및 위치
연구 장소
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Paris, 프랑스, 75003
- Centre de Santé au Maire-Volta
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Paris, 프랑스, 75012
- Centre d'examen de santé de la CPAM, antenne rue du Maroc
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Paris, 프랑스, 75012
- Consultation Policlinique de l'hôpital Saint-Antoine
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Paris, 프랑스, 75012
- Consultation Voyage de l'hôpital Saint-Antoine
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Paris, 프랑스, 75020
- CDAG de Belleville
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
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
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 상영
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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활성 비교기: 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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실험적: 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.
다른 이름들:
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Percentage of Patients Appropriately Seeking Care
기간: 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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공동 작업자 및 조사자
수사관
- 수석 연구원: Julie Bottero, MD, Hopital Saint-Antoine
간행물 및 유용한 링크
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
키워드
추가 관련 MeSH 약관
기타 연구 ID 번호
- IMEA 38
- 2011-A01603-38 (레지스트리 식별자: ANSM)
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
IPD 계획 설명
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
간경화에 대한 임상 시험
-
University Hospital, Basel, Switzerland아직 모집하지 않음
ELISA testing에 대한 임상 시험
-
Washington University School of MedicineThe Foundation for Barnes-Jewish Hospital종료됨린치 증후군 | 유전성 유방암 및 난소암미국
-
Medizinische Hochschule Brandenburg Theodor Fontane완전한
-
University of Oxford완전한
-
Saglik Bilimleri Universitesi완전한
-
Cumhuriyet UniversityKırıkkale University완전한
-
Nanfang Hospital, Southern Medical University모병
-
Shahid Beheshti University of Medical Sciences완전한