A Comparative Analysis of Ultrasound's Accuracy in Diagnosing HC Using Histopathology as Gold Standard
1 other identifier
observational
90
1 country
1
Brief Summary
The study aims to evaluate the accuracy of ultrasound in diagnosing hepatocellular carcinoma (HCC), using histopathology as the gold standard. It addresses HCC's high global incidence and the utility of ultrasound as a non-invasive, cost-effective screening tool. Despite ultrasound's accessibility, its diagnostic limitations necessitate further investigation to improve clinical outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Mar 2024
Shorter than P25 for all trials
1 active site
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
Study Start
First participant enrolled
March 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2024
CompletedFirst Submitted
Initial submission to the registry
December 19, 2024
CompletedFirst Posted
Study publicly available on registry
December 27, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
February 20, 2025
CompletedDecember 27, 2024
December 1, 2024
6 months
December 19, 2024
December 19, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
ultrasound
Sensitivity and Specificity analysis of Ultrasound as diagnostic tool, with histopathology as gold standard.
12 Months
Interventions
To determine the sensitivity of ultrasound in detecting HCC
Eligibility Criteria
aim is to check the accuracy of Ultrasound's in Diagnosing Hepatocellular Carcinoma Using Histopathology as Gold Standard
You may qualify if:
- Clinically suspected liver cancer patients undergoing ultrasound examination.
- Patients undergoing histopathological examination (liver biopsy or resection) for definitive diagnosis.
You may not qualify if:
- \- Patients with history of liver cancer treatment or inadequate data."
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Medcare International Hospital
Gujranwala, Punjab Province, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
December 19, 2024
First Posted
December 27, 2024
Study Start
March 1, 2024
Primary Completion
September 1, 2024
Study Completion
February 20, 2025
Last Updated
December 27, 2024
Record last verified: 2024-12
Data Sharing
- IPD Sharing
- Will not share