Upper GI disease Not Applicable
Conditions
Interventions
Patients are enrolled as indoor and outdoor patients and randomised in a way approved before and after patients consent. The specific catheter is inserted by either a specialised nurse or doctor.
Sponsors
Sahlgrenska University Hospital (Sweden)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Male or Female over 18 yrs in need of a central line 2. Patient has received information of the study and consent is given
Exclusion criteria
Exclusion criteria: Patient who has no need of central venous access
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Catheter treatment period: measured in 2014/15 approximately | — |
Secondary
| Measure | Time frame |
|---|---|
| Side effects such as thrombosis, thromophlebitis, pneumothorax, hemothorax, deep and surface infections: measured in 2014/15 approximately | — |
Countries
Sweden
Outcome results
None listed