Evaluation of spleen stiffness applicability and utility in a tertiary hospital.

Recruiting

• Conditions: HCV; MALFD; Portal hypertension; Liver cirrhosis; Liver test abnormalities; HBV; Liver disease

• Registration Number: NL-OMON24949
• Lead Sponsor: Foundation for Liver and Gastrointestinal Research (SLO) c/o Department of Hepatology & Gastroenterology Erasmus MC, University Medical Center Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 250

Inclusion Criteria

Patients aged 18 years or older visiting the liver ultrasound unit of the ErasmusMC.

Exclusion Criteria

Prior objection regarding the use of personal data for research

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Correlation spleen stiffness measurement in relation to the absence or presence of portal hypertension

Secondary Outcome Measures

Name	Time	Method
Predictors of spleen stiffness measurement success<br>Accuracy of spleen stiffness measurement <br>Predictors of accuracy of spleen stiffness measurement<br>Applicability of spleen stiffness measurement in patients with liver disease.