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Comparative Diagnostic performance of Alpha-1-Antitrypsin and AFP in the detection of hepatocellular carcinoma

Molecular And Serological Evaluation of Alpa-1- Antitrypsin (A1AT) in the different stages of Hepatocellular Carcinoma (HCC)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230813059136N1
Enrollment
10
Registered
2023-09-02
Start date
2021-05-02
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Investigate the role of Alpha -1- antitrypsin (A1AT) and Alpha-Fetoprotein (AFP) in hepatocellular carcinoma among Iraqi patients.. Alpha-1-antitrypsin deficiency,

Interventions

Control group: The control group, contains 100 healthy volunteers with unrelated healthy blood donors, free of any chronic diseases, living in the same geographical area recruited as normal healthy co
they were 78 males and 22 females with a mean age of 55.12 ± 11.36 years..

Sponsors

University of Sousse
Lead Sponsor
The university of sousse
Collaborator

Eligibility

Sex/Gender
All
Age
50 Years to 60 Years

Inclusion criteria

Inclusion criteria: This case-control study was conducted on 100 HCC patients being treated at the National Liver Institute Hospital, Baghdad University, Iraq. All of the participants were Iraqis. As control subjects, 100 age- and sex-matched healthy blood donors with no history of malignant or genetic diseases provided blood samples. Until analysis, blood and plasma samples were kept at 80 °C.

Exclusion criteria

Exclusion criteria: Individuals with a documented medical history of malignancy and genetic disorders were not included in the study. Individuals with a higher incidence of the disease in regions other than the liver were excluded from the study. Exclusions were made for patients who expired within the duration of the research.

Design outcomes

Primary

MeasureTime frame
Alpha -1- antitrypsin. Timepoint: Before intervention and 10 weeks after intervention. Method of measurement: The plasma A1AT level was measured by nephelometry using commercially available antibodies (MININEPH, Birmingham, UK), with an Array™ Protein System autoanalyzer (Beckman Instruments, Brea, California, USA).

Countries

Iraq

Contacts

Public ContactBassem Charfeddine

University of Sousse

doyen.fms@gmail.com73222108

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026