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Chronic Hepatitis D InfectionSITUHDVATIONNCT06248580

Find HDV and Determine Its Status in Turkey

An observational study of Chronic Hepatitis D Infection and Fibrosis, Liver, run by Yaşar Bayındır, MD at 2 sites in Turkey (Türkiye).

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
Anti Delta
How many people
20,000 participants
Where
2 sitesTurkey (Türkiye)
Study dates
11 Mar 2024to 1 Mar 2025
How long will I take part?
13 Months
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

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.

Who may be able to join

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

Who cannot join

  • There are no exclusion criteria in this study.

Trial locations and contacts

2 sites in 1 country.

Yaşar Bayındır, MD contact

00905323659909

yasar.bayindir@guven.com.tr

Mustafa Kemal Çelen, MD contact

00905336207022

Turkey (Türkiye)2 sites, 2 recruiting
  • Guven Hospital

    Ankara, 06850

    Yaşar Bayındır, MD, 00905323659909, yasarb44@hotmail.com

    Mustafa Kemal Çelen, MD

    Recruiting
  • Dicle University, Faculty of Medicine

    Diyarbakır

    Mustafa Celen, MD, 00905336207022, mkcelen@hotmail.com

    Cigdem Mermutluoglu, MD, 00905052252700, cigdemmermut@gmail.com

    Recruiting

Other trials in Turkey (Türkiye)

About this study

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

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.

Being tested
Anti Delta
Keywords
Chronic hepatitis D, Hepatocellular Carcinoma, Liver Cirrhosis
Medical subject headings
Liver Cirrhosis, Carcinoma, Hepatocellular, Hepatitis D, Chronic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Anti DeltaDiagnostic test

    Also called Fibroscan

    Anti Delta by ELISA

Study groups in NCT06248580
Study groupRoleWhat they receive
Family Physicians1. 250 Family Physicians
HDV Screening2. 20,000 HBsAg positive patients
Receives: Diagnostic Test: Anti Delta

What is being measured

The primary outcome is the main question the study is designed to answer.

  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.

    Measured: 01.04.2024-30.09.2024

Secondary outcomes (1)
  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.

    Measured: 01.04.2024-30.09.2024

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Feb 2024
  2. Study start11 Mar 2024
  3. Primary completion1 Feb 2025 (estimated)
  4. Study completion1 Mar 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Prospective
Enrolment
20,000 participants (estimated)
Target duration
13 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT06248580
Sponsor's protocol ID
Guven Health Group
Acronym
SITUHDVATION
Status last verified
Aug 2024
First submitted
31 Jan 2024
Last updated
12 Aug 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Study data will be shared with researchers periodically.

Questions about this trial

What is this clinical trial studying?

An observational study of Chronic Hepatitis D Infection and Fibrosis, Liver, run by Yaşar Bayındır, MD at 2 sites in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 12 Aug 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Yaşar Bayındır, MD (00905323659909, yasar.bayindir@guven.com.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The frequency of HDV in certain regions of Southern Anatolia (time frame: 01.04.2024-30.09.2024). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Aug 2024.

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