ClinicalTrials.gg
RecruitingNCT06248580SITUHDVATIONUpdated Aug 12, 2024

Find HDV and Determine Its Status in Turkey

An observational study in Chronic Hepatitis D Infection, Fibrosis, Liver and Hepatocellular Carcinoma, sponsored by Yaşar Bayındır, MD. Recruiting at 2 sites in Turkey. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-08-12.

Sponsored by Yaşar Bayındır, MD · Observational

From the registry’s dates

  • Primary completion was expected by Feb 2025, 1 year 9 months ago, but the record still lists the study as recruiting.
  • Started Mar 2024; still recruiting 2 years 8 months later.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
20,000
Ages
18 Years and older
Sex
All
01

Study 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.

Read the 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:

  • To determine the frequency and type of HDV in HBV patients (HDV/HCV co-infection).
  • Providing HBV, HCV, HDV and HIV awareness training to family physicians.
  • To determine the virological and liver fibrosis of patients with anti-Delta positivity.
  • To determine the status of patients with HBV infection who are followed by family physicians.
  • To ensure that patients with HDV infection are evaluated for liver cirrhosis and liver cancer.
  • To determine the HDV/HIV co-infection rate.
  • To determine the HDV/HCV co-infection rate.
  • Determining the vertical transmission rate in viral hepatitis and contributing to elimination by emphasizing the importance of this rate.

Study 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.

Number of Volunteers to Participate in the Study:

It is planned to include a total of 20,000 patients with HBsAg positivity from four provinces in this study.

Study Design:

Hepatitis Delta Virus infection poses a greater risk of developing both cirrhosis and liver cancer than other viral hepatitis agents. The Southeastern Anatolia region where HDV infection is most common in Turkey. It is planned to include four provinces (Diyarbakir, Batman, Mardin and Sanliurfa) in this study. In this study, family physicians will be reached through the Health Directorate of each province.

All Family Physicians will be educated about the prognosis and complications of HBV and especially HDV infection. The training will be carried out by the Infectious Diseases or Gastroenterology specialists of that province. Anti-Delta will be tested in all patients applying to health institutions. At the same time, all HBsAg positive patients followed by each family physician will be evaluated for the presence of HDV infection. All patients with anti-Delta positivity will be tested for HIV and HCV to determine their HDV/HIV co-infection and HDV/HCV co-infection status. Simultaneously, the liver fibrosis of patients with Anti-Delta positivity will be evaluated by the fibroscan method. Fibrosis-4 (FIB-4) and Child Pugh scoring will be performed on all patients simultaneously.

After receiving ethics committee approval for this study, the data collection process for family physicians' training and follow-up patients will be completed between April and July 2024. In total, it is anticipated to reach 250 Family Physicians in the entire region. In addition, demographic characteristics of HDV patients will be determined by reaching the Infectious Diseases and Gastroenterology Centers in four provinces. A five-question survey would be organized for all family physicians before and after the training in order to measure their knowledge level and evaluate the contribution of the training. This survey will be applied and analyzed via Slido.

After determining the biochemical and virological status of all HDV infections detected in four provinces, fibrosis of the liver will be measured with Fibroscan and FIB-4, which are non-invasive methods. As a result of the study, it is aimed to diagnose an estimated 1000 HDV-infected patients and score their liver fibrosis. It is aimed to complete the biochemical, virological, demographic and liver fibrosis status and statistical analyzes of all HDV-infected patients by 31.12.2024. The status of all patients in need of treatment or transplantation will be determined and their follow-up and treatment will be carried out in line with the recommendations of international and national treatment guidelines. The writing phase of all analyzed data will be completed and finalized by 31.01.2025.

One of the important reasons why both hepatitis B infection (HBV) and HDV infections are common is related to the fact that until recently vertical transmission was an important risk factor.

Both the diagnostic approach and follow-up and effective treatment options for HDV infections are still limited. It is also clearly known that HDV infection carries a higher risk of hepatocellular carcinoma (HCC) and cirrhosis than HBV infection. It is known that 90% of patients with viral hepatitis origin who are transplant candidates in our country have HDV infection.

02

Conditions studied

  • Chronic Hepatitis D Infection
  • Fibrosis, Liver
  • Hepatocellular Carcinoma
  • Cirrhosis, Liver
  • Transmission Vertical

Keywords

  • Chronic hepatitis D
  • Hepatocellular Carcinoma
  • Liver Cirrhosis
03

In context

Liver Cirrhosis

1,298 studies on the registry are indexed under Liver Cirrhosis; 338 are open to participants now.

This study's planned enrollment of 20,000 is above the median of 171 across 526 observational studies indexed under Liver Cirrhosis.

Browse Liver Cirrhosis studies →

Lead sponsor

Yaşar Bayındır, MD is the lead sponsor of 5 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study 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.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • There are no exclusion criteria in this study.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
20,000 participants (estimated)
Target follow-up
13 Months
Patient registry
Yes

Groups and cohorts

  • Family Physicians

    1. 250 Family Physicians

  • HDV Screening

    2. 20,000 HBsAg positive patients

    Diagnostic Test: Anti Delta

Interventions

  • Diagnostic testAnti Delta

    Anti Delta by ELISA

    Also known as: Fibroscan

06

What researchers measure

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

07

Study locations

2 of 2 sites recruiting
08

References and documents

Individual participant data

Plan to share: No — Study data will be shared with researchers periodically.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 12, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06248580
Lead sponsor
Yaşar Bayındır, MD
Collaborators
SOUTHEAST NEUROLOGY AND INFECTIOUS DISEASES SOCIETY, Gilead Sciences
Responsible party
Yaşar Bayındır, MD (Chief Physician, Prof. Dr., M.D., Guven Health Group) — Sponsor-investigator
First posted
Feb 8, 2024
Start date
Mar 11, 2024
Primary completion
Feb 1, 2025 (estimated)
Completion
Mar 1, 2025 (estimated)
Last update
Aug 12, 2024

Study contacts

Yaşar Bayındır, MD
Contact
yasar.bayindir@guven.com.tr
00905323659909
Mustafa Kemal Çelen, MD
Contact
00905336207022
Mustafa Kemal Çelen, MD
principal investigator · Dicle University, Medical Faculty, Department of Infectious Diseases

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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