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A Multicountry, Multicenter, Secondary Data Collection, Retrospective Observational Study to Describe the Characteristics and Management of Hepatocellular Carcinoma (HCC) Among Adults in the Middle East Region

Status: Recruiting
Location: See all (17) locations...
Study Type: Observational
SUMMARY

Hepatocellular carcinoma (HCC) is the sixth most commonly diagnosed cancer and the third reason for cancer-related death worldwide. Cirrhosis is a common risk factor of HCC, as it is found in approximately 70-90% of patients with HCC. Hepatitis C (HCV) and alcohol consumption represent the main causes of cirrhosis and HCC in Western countries; however, hepatitis B virus (HBV) is the leading cause of HCC and cirrhosis in East Asia and Africa. Moreover, HBV and HCV are considered the most common causes of HCC in about 80%-90% of patients. In addition, steatotic liver disease (SLD) is considered one of the main causes of HCC and cirrhosis. Unfortunately, the burden of HCC is great in Middle Eastern and North African (MENA) countries because of the high prevalence of HCV and HBV and the increasing incidence of SLD and metabolic-associated steatohepatitis (MASH). Several studies illustrated that there are great disparities in the survival rate of patients with HCC according to patient characteristics such as gender, age, and socioeconomic status. In addition, the etiology of HCC may impact the survival and the response to treatment. Moreover, the incidence of HCC could be decreased by the prevention and/or appropriate management of HCC risk factors, especially HBV, HCV infections, and SLD. Therefore, understanding the etiology, patient characteristics, pathogenesis, and optimal management of HCC in the region is considered of prime importance to improve the patient journey of HCC in the MENA region. The Middle East encompasses countries with varying levels of healthcare development and resources. There is a significant disparity in access to diagnostic tools, therapeutic options, and liver transplantation services. While some countries possess advanced healthcare systems with state-of-the-art facilities, others face challenges such as limited healthcare infrastructure, shortage of specialized healthcare professionals, and inadequate screening programs. These disparities significantly affect the early detection, management, and outcomes of HCC patients. This study aims to assess the etiology, clinical and tumor characteristics, and treatments received for HCC, as well as clinical outcomes (OS, PFS) in different countries in the MENA region.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Patients with a radiological or histopathological confirmed diagnosis with HCC in any stage of the tumor between 1st January 2015 and 31st December 2023 (defined as index date).

• Patient or next of kin/legal representative (for deceased patients at study entry, unless a waiver is granted) willing and able to provide written informed consent according to the local regulations

• Age 18 years or older, and a lawful adult in the country at the index date

• Patients with medical records, including etiology, laboratories, radiological, and treatment details will be collected from the participating sites.

• Patients with medical records covering at least a 6-month follow-up period, defined as the time from the index date (the date of the first diagnosis) to the earliest of the following: the patient's death, the last medical record entry, or the data extraction date. Additionally, patients who died within this 6-month period will also be included.

Locations
Other Locations
Egypt
Research Site
NOT_YET_RECRUITING
Al Mansurah
Research Site
NOT_YET_RECRUITING
Dakahlia
Research Site
NOT_YET_RECRUITING
Damietta
Research Site
NOT_YET_RECRUITING
Menouf
Kuwait
Research Site
NOT_YET_RECRUITING
Kuwait City
Morocco
Research Site
NOT_YET_RECRUITING
Rabat
Qatar
Research Site
NOT_YET_RECRUITING
Doha
Saudi Arabia
Research Site
NOT_YET_RECRUITING
Dammam
Research Site
NOT_YET_RECRUITING
Jeddah
Research Site
NOT_YET_RECRUITING
Mecca
Research Site
NOT_YET_RECRUITING
Riyadh
Turkey
Research Site
NOT_YET_RECRUITING
Ankara
Research Site
NOT_YET_RECRUITING
Erzurum
Research Site
NOT_YET_RECRUITING
Istanbul
Research Site
NOT_YET_RECRUITING
Izmir
United Arab Emirates
Research Site
NOT_YET_RECRUITING
Abu Dhabi
Research Site
RECRUITING
Al Ain City
Contact Information
Primary
AstraZeneca Clinical Study Information Center
information.center@astrazeneca.com
1-877-240-9479
Time Frame
Start Date: 2026-07-14
Estimated Completion Date: 2027-11-30
Participants
Target number of participants: 4000
Sponsors
Leads: AstraZeneca

This content was sourced from clinicaltrials.gov