Register non-cirrhotic portal vein thrombosis

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00000810

Enrollment

Registered

2016-04-05

Start date

2016-02-15

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

I81

Interventions

Group 1: Documentation of the follow up of non-cirrhotic portal vein thrombosis with medical or interventional therapy. Registration of effectivity and complications of the therapy.

Eligibility

Sex/Gender

All

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: non-cirrhotic portal vein thrombosis

Exclusion criteria

Exclusion criteria: liver cirrhosis, HCC

Design outcomes

Primary

Measure	Time frame
Variceal bleeding	—

Secondary

Measure	Time frame
Extent/regression of thrombosis - Appearance of Cavernoma - Abdominal pain and abdominal disorders - hypersplenism (hemoglobin < 11 g/dl, thrombocytes < 100 Tsd/µl) - portal biliopathy - overall survival	—

Countries

Germany

Contacts

Public ContactMichael Schultheiß

Universitätsklinikum Freiburg

michael.schultheiss@uniklinik-freiburg.de0761-270-34010

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026