First attempt success ratio of intravenous cannulation with the Veinplicity®
- Conditions
- Difficult intravenous accessPeripheral intravenous cannulation
- Registration Number
- NL-OMON25489
- Lead Sponsor
- Catharina Hospital; department of anesthesiology, intensive care and pain medicine; Michelangelolaan 2; 5623 EJ Eindhoven; The Netherlands.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 125
In order to be eligible to participate in this study, a patient must meet all of the following criteria: patients must be in the age of 18 years or older; patients with a medium risk profile on the A-DIVA scale (score 2 or 3); and patients must be conscious and be able to adequately answer questions.
A potential patient who meets any of the following criteria will be excluded from participation in this study: patients in which an intravenous catheter is already inserted on the ward; patients who are unwilling or unable to provide consent to participate; patients with medical devices in the body (pacemaker, ICD, trans-cerebral electrode placement, electrode placement that applies current to the carotid sinus region, other neurostimulators); and patients who do not understand questions or generate adequate data, due to physical or communicational disorders.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method