I87.2
Conditions
Interventions
Group 1: Control group: 20 patients after venous recanalization:
Treatment anticoagulation + compression stockings class 2 (Standard of Care)
Group 2: Intervention group: 20 patients after venous reca
Sponsors
Universitätsklinikum Aachen
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.Patients with an indication for surgery Supply of the leg veins 2. Patients with unilateral pathology
Exclusion criteria
Exclusion criteria: 1. People who are not fully capable of giving consent are able to determine essence, meaning and Understand the scope of the study 2. patient with re-operations of the same venous pathology 3. peripheral arterial disease 4. Contraindication to anticoagulation 5. Sores on the foot, so the foot pump cannot be used be created there
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The aim is to show that therapy using a pneumatic foot pump is a useful addition to the already established therapy for chronic venous obstruction. These effects would be reflected in both clinically recorded parameters (leg circumference, sonography, etc.) and the subjective well-being of the patients (questionnaires). | — |
Secondary
| Measure | Time frame |
|---|---|
| As well as the subjective well-being of the patients (questionnaires). | — |
Countries
Germany
Contacts
Public ContactMohammad Barbati
Universitätsklinikum Aachen
Outcome results
None listed