Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
66 participants
OBSERVATIONAL
2025-10-01
2027-11-01
Brief Summary
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Detailed Description
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In these cases, locoregional therapies such as transarterial chemoembolization (TACE) and microwave ablation (MWA) play a pivotal role. Both techniques aim to achieve local tumor control and improve patient survival. TACE induces ischemic necrosis through targeted delivery of chemotherapeutic agents combined with arterial embolization, whereas MWA achieves tumor destruction by generating high-frequency electromagnetic waves that produce thermal coagulative necrosis. Accurate assessment of treatment response is essential for guiding clinical decisions and predicting outcomes. Conventional imaging-based response criteria, such as RECIST and mRECIST, primarily focus on changes in lesion diameter. However, these methods may not fully reflect the extent of tumor necrosis or viable residual tissue . In this context, CT-based volumetric measurements have emerged as a more objective and sensitive tool for evaluating therapeutic response after locoregional treatment. Volumetric analysis provides a three-dimensional assessment of tumor burden and may bet ter correlate with treatment efficacy and prognosis compared to traditional linear measurements. Therefore, this study aims to investigate the role of CT volumetric measurement of HCC after TACE or microwave ablation in evaluating treatment response and predicting clinical outcomes .
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Ct
Ct volume measurement of HCC after TACE or MWA
Eligibility Criteria
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Inclusion 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.
Exclusion Criteria
* Patients with contraindications to iodinated contrast or TACE.
* Patients with severe comorbid illness that precludes participation.
* Patients refuse to provide informed consent.
18 Years
ALL
No
Sponsors
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Assiut University
OTHER
Responsible Party
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Ahmed Saber Hamed Ahmed
Assistant lecturer
Central Contacts
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Other Identifiers
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Ct volume measaurement of HCC
Identifier Type: -
Identifier Source: org_study_id
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