About this trial
The aim of these study to determine the prevalence of hepatitis Delta virus (HDV) infections and the prognosis of HDV patients in Turkey's southeast. The investigators intend to arrange training sessions for 250 family physicians in Diyarbakir, Batman, Mardin, and Sanliurfa in order to determine those goals. The investigators will talk about diagnosing hepatitis B virus (HBV), HDV, hepatitis C virus (HCV), and Human Immunodeficiency virus (HIV) infections during these events. To ensure that patients with simultaneous HDV infection are evaluated for HIV/HCV and to detect liver fibrosis with a non-invasive method.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Adults (Age≥18)
Being HBsAg positive for at least six months
Being a citizen of the Republic of Türkiye
Disqualifiers
There are no exclusion criteria in this study.
Trial population
To ensure that 20,000 patients with HBsAg positivity in Diyarbakir, Mardin, Batman and Sanliurfa are evaluated for HDV infection. To investigate HDV positive patients for liver fibrosis using the fibroscan method.
Trial design
Other
Prospective
Treatments tested in this trial
Anti Delta
Diagnostic testAnti Delta by ELISA
Treatment groups
Trial outcomes
Primary outcomes
The frequency of HDV in certain regions of Southern Anatolia
The primary endpoint of this study is to determine the frequency of HDV in certain regions of Southern Anatolia, and the virological and liver fibrosis status of patients with HDV infection.
Secondary outcomes
The rate of HIV and HCV co-infection in HDV positive patients
To determine the rate of HIV and HCV co-infection in HDV positive patients and to determine the demographic characteristics of HDV infected cases.
Sponsors and contacts
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Yaşar Bayındır, MD
Lead sponsor
Guven Health Group
Sponsor institution
SOUTHEAST NEUROLOGY AND INFECTIOUS DISEASES SOCIETY
Collaborator
Gilead Sciences
Collaborator