First attempt success ratio of intravenous cannulation with the Veinplicity®

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON24775

Enrollment

125

Registered

2017-05-22

Start date

2017-09-01

Completion date

Unknown

Last updated

2024-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Difficult intravenous access, unsuccessful attempt to insert a peripheral intravenous catheter.

Interventions

In patients in the intervention group, a peripheral intravenous catheter will be inserted with the aid of the Veinplicity® device. For the control group, a historical cohort will be used. The Veinplic

Eligibility

Inclusion criteria

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

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.

Design outcomes

Primary

Measure	Time frame
The primary outcome is the first attempt success ratio of peripheral intravenous catheter placement with the use of the Veinplicity® device, when compared to the traditional landmark technique, in patients with a medium-risk profile according to the A-DIVA scale. The outcome of interest is to reach a success ratio of 95% upon inserting a peripheral intravenous catheter by using the Veinplicity® device, in patients with a medium-risk profile according to the A-DIVA scale.	—

Measure

Time frame

The primary outcome is the first attempt success ratio of peripheral intravenous catheter placement with the use of the Veinplicity® device, when compared to the traditional landmark technique, in patients with a medium-risk profile according to the A-DIVA scale. The outcome of interest is to reach a success ratio of 95% upon inserting a peripheral intravenous catheter by using the Veinplicity® device, in patients with a medium-risk profile according to the A-DIVA scale.

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Secondary

Measure	Time frame
As secondary objectives, we are interested in the effects on: The time needed for intravenous cannulation; Patients satisfaction; Pain score upon intravenous cannulation; Practitioners satisfaction; The relation between the success ratio and patients demographics (age, sex, length, weight, skin color, dominant side, A-DIVA score, medical history and comorbidities); The relation between the success ratio and procedure related data (size of the vein, size of the inserted catheter, side of cannulation, site of cannulation).	—

Measure

Time frame

As secondary objectives, we are interested in the effects on: The time needed for intravenous cannulation; Patients satisfaction; Pain score upon intravenous cannulation; Practitioners satisfaction; The relation between the success ratio and patients demographics (age, sex, length, weight, skin color, dominant side, A-DIVA score, medical history and comorbidities); The relation between the success ratio and procedure related data (size of the vein, size of the inserted catheter, side of cannulation, site of cannulation).

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Contacts

Public ContactF.H.J. van Loon

Catharina Hospital, Department of anesthesiology

rick.v.loon@catharinaziekenhuis.nl040-2399111 (beeper 115201)

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)