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First attempt success ratio of intravenous cannulation with the Veinplicity®

Completed
Conditions
intraveneuze toegang, perifeer
Difficult intravenous access / (peripheral) intravenous cannulation
10062915
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
Inclusion Criteria

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.

Exclusion Criteria

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
NameTimeMethod
<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
NameTimeMethod
<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>
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