Chronic venous insufficiency
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Presence of venous insufficiency (Group I) Presence of post-thrombotic syndrome (Group II) Absence of venous insufficiency (Group III)
Exclusion criteria
Exclusion criteria: Acute thrombosis Pregnancy (not due to risk to the pregnant individual or the unborn child, but because of the potential influence on the results) Lack of capacity to provide informed consent Insufficient ability to communicate in German Participation in another study within the previous 4 weeks
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of the effectiveness and reproducibility of the respective measurement methods, assessed during a single study visit, with performance of the three measurement procedures: PPG, LRR, and DPG. | — |
Secondary
| Measure | Time frame |
|---|---|
| Correlation of the results with quality-of-life questionnaires and findings from the clinical examination. Comparison of the results (primary endpoint) with clinical assessment (CEAP, VCSS) and questionnaires (CIVIQ). | — |
Countries
Germany
Contacts
Venenpraxis Wunstorf