Non-invasive quantification of liver fibrosis with ultrasound: pilot

Non-invasive quantification of liver fibrosis with ultrasound: pilot - Non-invasive quantification of liver fibrosis

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON37760

Enrollment

Registered

2012-05-04

Start date

2012-05-04

Completion date

Unknown

Last updated

2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

liver fibrosis liver scarring

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Group 1: 25 healthy volunteers, age 25-70 years, BMI 20-40 Group 2: 25 patients with histologically confirmed cirrhosis, age > 18 years

Exclusion criteria

Exclusion criteria: Group 1 History of liver disease Excessive alcohol use (> 25 consumptions per week for men, > 10 consumptions per week for women)

Design outcomes

Primary

Measure	Time frame
The main study outcomes are: • Reference intervals • Intra- and interobserver variability To this end, the following variables will be measured / calculated: strain (for elastography) and inhomogeneity (for ASQ), their variances, the corresponding effect size and coefficients of agreement.	—

Secondary

Measure	Time frame
nvt	—

Countries

Netherlands

Outcome results