CT Volume Measurement of Hepatocellular Carcinoma
Ct Volume Measurement of Hepatocellular Carcinoma After Transarterial Chemoembolization (TACE) or Microwave Ablation (MWA)
1 other identifier
observational
66
0 countries
N/A
Brief Summary
The aim of this study is to evaluate the role of CT volumetric measurement in assessing treatment response of hepatocellular carcinoma (HCC) following trans arterial chemoembolization (TACE) or microwave ablation (MWA)
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Oct 2025
Typical duration for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 12, 2025
CompletedFirst Posted
Study publicly available on registry
September 19, 2025
CompletedStudy Start
First participant enrolled
October 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
November 1, 2027
September 19, 2025
September 1, 2025
2 years
September 12, 2025
September 17, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Ct volume measurent of hepatocellular carcinoma after Transarterial chemoembolization or microwave ablation
At enrollment, all patients will undergo a comprehensive clinical assessment, including full medical history with emphasis on risk factors for hepatocellular carcinoma triphasic CT scan of the liver, which will serve as the reference for tumor volume (by cm3 or cc), number, and distribution prior to TACE or MWA.
Baseline
Interventions
Ct volume measurement of HCC after TACE or MWA
Eligibility Criteria
All patients admitted to Assiut University Hospital, Egypt during the period of the study and fulfil the inclusion criteria
You may qualify if:
- Adult patients (≥18 years) with a confirmed diagnosis of HCC based on AASLD or EASL criteria.
- Patients deemed unresectable by the multidisciplinary tumor board.
- Patients scheduled for TACE as the primary locoregional therapy.
- Preserved liver function (Child-Pugh class A or B).
- Adequate renal function to permit contrast-enhanced CT.
You may not qualify if:
- Patients with extrahepatic metastases or portal vein thrombosis.
- Patients with contraindications to iodinated contrast or TACE.
- Patients with severe comorbid illness that precludes participation.
- Patients refuse to provide informed consent.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant lecturer
Study Record Dates
First Submitted
September 12, 2025
First Posted
September 19, 2025
Study Start
October 1, 2025
Primary Completion (Estimated)
October 1, 2027
Study Completion (Estimated)
November 1, 2027
Last Updated
September 19, 2025
Record last verified: 2025-09