King Abdullah bin Abdulaziz University Hospital
Riyadh, Saudi Arabia
NCT Number: NCT06313047
The study included 81 HCC patients, both male and female. Prior to being assessed for eligibility, each recruited patient with HCC received a comprehensive review of their medical history, physical status, and laboratory results. Every research participant take part in the experiment and provided written informed consent.
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Notify Me20 year–75 year
All sexes
Observational
Riyadh, Saudi Arabia
All patients had their baseline viral indicators for HBV and HCV evaluated. Additionally, blood samples were taken for genotyping. All patients underwent evaluations of their kidney, liver, and alpha fetoprotein (AFP) functions, as well as their complete blood count (CBC), at both the baseline and follow-up appointments. To evaluate the efficacy of TACE, triple pelvic abdominal CT scans were performed both prior to and one month later. Using triphasic pelviabdominal CT, patients who achieved complete response (CR) were monitored for up to 13 months following chemotherapy in order to identify recurrence. Follow-up appointments were planned to identify patients responces or any negative effects.
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
each recruited patient with HCC received a comprehensive review of their medical history, physical status, and laboratory results.
Other names: Dox
Time frame: 1 year
Genotyping
Time frame: 1 year
Genotyping
Rehab Werida
Other
Pharmacogenetic of Doxorubicin in Patients With Hepatocellular Carcinoma: A Prospective Cohort Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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