Trials / Terminated
TerminatedNCT01020461
Evaluation of Accuvein in Adult Patients
Evaluation of Accuvein for Blood Sampling and for Intravenous Catheter Placement in Adult Patients
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 522 (actual)
- Sponsor
- Hopital Foch · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to evaluate the effectiveness of Accuvein to facilitate venous blood sampling and placement of peripheral intravenous catheters in adults. This clinical protocol is designed to determine whether using Accuvein increases the ease and efficiency of venous cannulation (as perceived by the operator), decreases the time to effective cannulation, decreases the number of sticks, and decreases the patient's perception of the pain.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Accuvein | Accuvein will be used to facilitate venous blood sampling |
| DEVICE | Accuvein | Accuvein will be used to facilitate peripheral IV catheter placement |
Timeline
- Start date
- 2010-01-01
- Primary completion
- 2013-04-01
- Completion
- 2013-04-01
- First posted
- 2009-11-25
- Last updated
- 2016-09-23
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT01020461. Inclusion in this directory is not an endorsement.