RecruitingNCT07351669
A Multicenter Prospective Study on the Performance of Spectral CT for Evaluating Treatment Response After TACE in Hepatocellular Carcinoma
The Performance of Spectral CT in Evaluating Treatment Response After Transarterial Chemoembolization for Hepatocellular Carcinoma: The SpecTRAIL Study
Sponsor
Zhongda Hospital
Enrollment
250 participants
Start Date
Jan 20, 2026
Study Type
OBSERVATIONAL
Conditions
Summary
By comparing the diagnostic accuracy of spectral CT and conventional CT in evaluating treatment response efficacy after TACE, this study aims to investigate the diagnostic performance of spectral CT in assessing treatment response following TACE for hepatocellular carcinoma.
Eligibility
Min Age: 18 YearsMax Age: 75 Years
Inclusion Criteria10
- Voluntary participation and ability to sign informed consent (post-TACE);
- Age between 18 and 75 years;
- Diagnosed as HCC based on pathology or clinical criteria, with a BCLC stage of A or B;
- Patients undergo contrast-enhanced spectral CT 4-8 weeks after treatment and are assessed as complete response on conventional CT images;
- Patients are scheduled to undergo surgical resection within one month, or DSA hepatic arteriography or contrast-enhanced MRI within one week. If none of these were planned, the patients were scheduled for imaging follow-up (CT or MRI) every 3 months (±15 days) for at least one year.
- Voluntary participation and ability to sign informed consent (post-TACE, cTACE or DEB-TACE);
- Age between 18 and 75 years;
- Diagnosed as HCC based on pathology or clinical criteria, with a BCLC stage of A or B;
- Patients plan to undergo liver tumor resection following TACE downstaging therapy;
- Contrast-enhanced spectral CT was performed within 7 days before liver resection, after completion of TACE down-staging treatment.
Exclusion Criteria4
- Contraindications to contrast-enhanced CT or contrast-enhanced MRI;
- Presence of extrahepatic malignancies;
- History of radiotherapy;
- Poor image quality or incomplete clinical/imaging data; Withdrawal from the study midway.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07351669
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