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Non-invasive Measurement of Hepatic Fibrosis in Patients Using Methotrexate.

Non-invasive Measurement of Hepatic Fibrosis in Patients Using Methotrexate. - Measurement of Hepatic Fibrosis in Patients Using Methotrexate.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON30803
Enrollment
1600
Registered
2007-07-05
Start date
2008-05-01
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

Liver damage en Liver disease

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Patiënts with Rheumatoid Arthritis - Use of Methotrexate - Disturbance of liver enzymes > 1,7 times upper limit - > 18 years.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Non-invasive Assessment of Fibrosis or Cirrhosis during treatment with Methotrexate in patients with Rheumatoid Arthritis and/or Psoriasis with the Fibroscan.

Secondary

MeasureTime frame
Incidence of liver enzyme disturbances in patients treated with Methotrexate for Rheumatoid Arthritis and Psoriasis. Incidence of Fibrosis or Cirrhosis in patients treated with Methotrexate for Rheumatoid Arthritis and Psoriasis.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)