healthy volutneers
Conditions
Interventions
Group 1: Different bonding techniques are compared with each other, but there is no venous puncture of the test persons. The plastic tube of the cannula is cut of.
Arm 1: prefabricated fixation devi
Sponsors
Uniklinik Freiburg Klinik für Anästhesiologie und Intensivmedizin
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: healthy volunteers
Exclusion criteria
Exclusion criteria: Lack of voluntariness, cortisone intake, skin diseases
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary endpoint : maximum force required [ Newton] to dislocate a peripheral intravenous cannula. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints: - mean force and impulse force ie for dislocation of a peripheral intravenous cannula - subjective assessment of the test subjects regarding the forces leading to the dislocation | — |
Countries
Germany
Contacts
Public ContactSebastian Heinrich
Uniklinik Freiburg Klinik für Anästhesiologie und Intensivmedizin
Outcome results
None listed