Indication for peripheral intravenous cannulation, regardless the medical specialism or type of surgery they are admitted for.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria: subjects must be in the age of 18 years or older; subjects must be conscious and be able to adequately answer questions.
Exclusion criteria
Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: when an intravenous catheter is already inserted on the ward; are unwilling or unable to provide consent to participate; do not understand questions or generate adequate data, due to physical or communicational disorders.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective is stated as the first attempt success rate of peripheral intravenous cannulation. | — |
Secondary
| Measure | Time frame |
|---|---|
| As secondary objectives, we are interested in the effects of the Venflon™ (Pro Safety with or without the BD InstaFlash™ Needle Technology) on the time needed for intravenous cannulation, the total number of attempts needed for successful cannulation, patients and practitioners satisfaction, pain score upon intravenous cannulation, practitioners satisfaction, and complications or side effects. | — |
Contacts
Catharina Ziekenhuis