NCT07183566

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

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
66

participants targeted

Target at P25-P50 for all trials

Timeline
16mo left

Started Oct 2025

Typical duration for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress34%
Oct 2025Nov 2027

First Submitted

Initial submission to the registry

September 12, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 19, 2025

Completed
12 days until next milestone

Study Start

First participant enrolled

October 1, 2025

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2027

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2027

Last Updated

September 19, 2025

Status Verified

September 1, 2025

Enrollment Period

2 years

First QC Date

September 12, 2025

Last Update Submit

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

CtDEVICE

Ct volume measurement of HCC after TACE or MWA

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Carcinoma, Hepatocellular

Condition Hierarchy (Ancestors)

AdenocarcinomaCarcinomaNeoplasms, Glandular and EpithelialNeoplasms by Histologic TypeNeoplasmsLiver NeoplasmsDigestive System NeoplasmsNeoplasms by SiteDigestive System DiseasesLiver Diseases

Central Study Contacts

Ahmes Saber Hamed, Master

CONTACT

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