Find HDV and Determine Its Status in Turkey

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorYaşar Bayındır, MD

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 volunteers

Qualifiers

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

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Anti Delta

    Diagnostic test

    Anti Delta by ELISA

Treatment groups

20,000 Participants
are divided into 2 treatment groups
Group A: Family Physicians0 interventions
Group B: HDV Screening1 intervention

Trial outcomes

Primary outcomes

1

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.

Time frame
01.04.2024-30.09.2024

Secondary outcomes

1

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.

Time frame
01.04.2024-30.09.2024

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Yaşar Bayındır, MD

Lead sponsor

Guven Health Group

Sponsor institution

SOUTHEAST NEUROLOGY AND INFECTIOUS DISEASES SOCIETY

Collaborator

Gilead Sciences

Collaborator