First attempt success ratio of intravenous cannulation with the Veinplicity®
- Conditions
- intraveneuze toegang, perifeerDifficult intravenous access / (peripheral) intravenous cannulation10062915
- Registration Number
- NL-OMON44449
- Lead Sponsor
- Catharina-ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- 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);
* 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 with medical devices in the body (pacemaker, ICD, trans-cerebral electrode placement, electrode placement that applies current to the carotid sinus region, other neurostimulators);
* Patients who do not understand questions or generate adequate data, due to physical or communicational disorders.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary outcome is the first attempt success ratio of peripheral<br /><br>intravenous catheter placement with the use of the Veinplicity® device, when<br /><br>compared to the traditional landmark technique, in patients with a medium-risk<br /><br>profile according to the A-DIVA scale. The outcome of interest is to reach a<br /><br>success ratio of 90% upon inserting a peripheral intravenous catheter by using<br /><br>the Veinplicity® device, in patients with a medium-risk profile according to<br /><br>the A-DIVA scale. </p><br>
- Secondary Outcome Measures
Name Time Method <p>As secondary objectives, we are interested in the effects on:<br /><br>* The time needed for intravenous cannulation;<br /><br>* Patients satisfaction;<br /><br>* Pain score upon intravenous cannulation;<br /><br>* Practitioners satisfaction;<br /><br>* The relation between the success ratio and patients demographics (age, sex,<br /><br>length, weight, skin color, dominant side, A-DIVA score, medical history and<br /><br>comorbidities);<br /><br>* The relation between the success ratio and procedure related data (size of<br /><br>the vein, size of the inserted catheter, side of cannulation, site of<br /><br>cannulation).</p><br>