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Recruiting NCT07782632

NCT07782632 Liver Volume Metrics for Predicting Immunotherapy Prognosis in Unresectable Hepatocellular Carcinoma

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Clinical Trial Summary
NCT ID NCT07782632
Status Recruiting
Phase
Sponsor Anhui Provincial Hospital
Condition Hepatocellular Carcinoma (HCC)
Study Type OBSERVATIONAL
Enrollment 467 participants
Start Date 2019-01-01
Primary Completion 2026-12-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 75 Years
Study Type OBSERVATIONAL
Interventions
Baseline Liver Volume Volumetric Analysis

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 467 participants in total. It began in 2019-01-01 with a primary completion date of 2026-12-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This multicenter retrospective cohort study aims to evaluate the prognostic value of functional liver volume and total liver volume in patients with unresectable hepatocellular carcinoma (HCC) undergoing immunotherapy. The study explores whether baseline liver volume metrics can effectively predict survival outcomes and treatment responses in this patient population to assist in clinical decision-making.

Eligibility Criteria

Inclusion Criteria: * Age \>= 18 years. * Clinically or histologically confirmed unresectable hepatocellular carcinoma (HCC). * Received immunotherapy as part of their tumor treatment regimen. * Availability of high-quality baseline pre-treatment imaging data suitable for functional liver volume and total liver volume segmentation. * Complete clinical and follow-up survival data. Exclusion Criteria: * \- Prior surgical resection or liver transplantation for HCC. * Co-existence of other concurrent primary malignant tumor types. * Severe image artifacts or technical limitations that prevent robust liver volume quantification. * Incomplete medical records, missing key baseline clinical data, or loss to follow-up.

Contact & Investigator

Central Contact

Jizhou Wang, MD

✉ wangjoe@ustc.edu.cn

📞 +86-551-62282931

Frequently Asked Questions

Who can join the NCT07782632 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Hepatocellular Carcinoma (HCC). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07782632 currently recruiting?

Yes, NCT07782632 is actively recruiting participants. Contact the research team at wangjoe@ustc.edu.cn for enrollment information.

Where is the NCT07782632 trial being conducted?

This trial is being conducted at Hefei, China.

Who is sponsoring the NCT07782632 clinical trial?

NCT07782632 is sponsored by Anhui Provincial Hospital. The trial plans to enroll 467 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology