- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning 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.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
-
-
Paris, Frankrike, 75003
- Centre de Santé au Maire-Volta
-
Paris, Frankrike, 75012
- Centre d'examen de santé de la CPAM, antenne rue du Maroc
-
Paris, Frankrike, 75012
- Consultation Policlinique de l'hôpital Saint-Antoine
-
Paris, Frankrike, 75012
- Consultation Voyage de l'hôpital Saint-Antoine
-
Paris, Frankrike, 75020
- CDAG de Belleville
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
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
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Undersökning
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: ELISA testing
HBV infection status determined by enzyme-linked immuno-assay (ELISA)
|
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).
|
|
Experimentell: Rapid testing
HBV infection status determined initially by a rapid test, then confirmed by enzyme-linked immuno-assay (ELISA).
|
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.
Andra namn:
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Percentage of Patients Appropriately Seeking Care
Tidsram: 6 months
|
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
|
Samarbetspartners och utredare
Samarbetspartners
Utredare
- Huvudutredare: Julie Bottero, MD, Hôpital Saint-Antoine
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
- Matsmältningssystemets sjukdomar
- Patologiska processer
- RNA-virusinfektioner
- Virussjukdomar
- Infektioner
- Blodburna infektioner
- Smittsamma sjukdomar
- Neoplasmer efter histologisk typ
- Neoplasmer
- Neoplasmer efter plats
- Adenocarcinom
- Carcinom
- Neoplasmer, körtel och epitel
- Neoplasmer i matsmältningssystemet
- Leversjukdomar
- Hepatit, Viral, Human
- Hepadnaviridae-infektioner
- DNA-virusinfektioner
- Neoplasmer i levern
- Enterovirusinfektioner
- Picornaviridae-infektioner
- Fibros
- Hepatit B
- Hepatit
- Karcinom, hepatocellulärt
- Hepatit A
- Levercirros
Andra studie-ID-nummer
- IMEA 38
- 2011-A01603-38 (Registeridentifierare: ANSM)
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
IPD-planbeskrivning
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