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Clinical Trials/NCT06248580
NCT06248580RecruitingNot Applicable

Find HDV and Determine Its Status in Turkey "SITU(HD)VATION"

Yaşar Bayındır, MD2 sites in 1 country20,000 target enrollmentStarted: March 11, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
20,000
Locations
2
Primary Endpoint
The frequency of HDV in certain regions of Southern Anatolia

Study Overview

Brief Summary

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.

Detailed Description

Study Objectives:

The aim of these study to determine the prevalence of 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 HBV, HDV, HCV, and 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.

Primary Objectives:

To reveal the status of HDV infection in Turkey within the framework of the national hepatitis elimination program by providing training to family physicians.

Second Objectives:

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Adults (Age≥18)
  • Being HBsAg positive for at least six months
  • Being a citizen of the Republic of Türkiye

Exclusion Criteria

  • There are no exclusion criteria in this study.

Outcomes

Primary Outcomes

The frequency of HDV in certain regions of Southern Anatolia

Time Frame: 01.04.2024-30.09.2024

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(01.04.2024-30.09.2024)

Investigators

Sponsor
Yaşar Bayındır, MD
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Yaşar Bayındır, MD

Chief Physician, Prof. Dr., M.D.

Guven Health Group

Study Sites (2)

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