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Hepatocellular Carcinoma Registry for Turkey (3K Trial)

Profile of the Hepatocellular Carcinoma Patients in Turkey

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01473121
Enrollment
600
Registered
2011-11-17
Start date
2012-08-13
Completion date
2018-07-12
Last updated
2019-07-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatocellular Carcinoma

Keywords

Hepatocellular carcinoma, Registry, Turkey

Brief summary

This registry study is national, multi-center, prospective study without any interventions to the treatment strategies and/or decisions of the investigators. It is designed in order to determine the general profile of HCC patients in Turkey. Socio-demographic characteristics, family history, medical history and treatment pattern of HCC patients will be evaluated.

Interventions

OTHERNo Intervention

All treatment options (inc. surgery, TACE, drugs) will be registered.

Sponsors

Bayer
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* To be diagnosed with hepatocellular carcinoma in last 3 months * To be older than 18 years old * To sign informed consent form (ICF)

Exclusion criteria

* Patients that does not sign or withdraw informed consent form. * According to investigator's opinion; existence of any situation/condition that will significantly complicate patient follow up. * Currently or previously taking part in 3K observational study

Design outcomes

Primary

MeasureTime frameDescription
Descriptive analysis of HCC risk factorsBaselinei.e. smoking and alcohol consumption status; family history for hepatitis, HCC, and other malignancies; history of hepatic disease and blood transfusion; concomitant diseases; treatments applied
Descriptive analysis of clinical profile of newly diagnosed HCC patientsBaseline

Secondary

MeasureTime frame
Descriptive analysis of clinical characteristics of HCC patientsUp to approximately 5 years
Number of participants with underlying liver disease and family historyBaseline
Number of participants with adverse eventsUp to approximately 5 years
Overall survival time since diagnosisUp to approximately 5 years
Descriptive analysis of tumor propertiesUp to approximately 5 years
Treatment options as applied by doctors to HCC patientsUp to approximately 5 years
Descriptive analysis of demographic characteristics of HCC patientsBaseline

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026