Trials / Terminated
TerminatedNCT02015845
Evaluation of Accuvein in Obese Patients
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 26 (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 placement of peripheral intravenous catheters in obese patients. 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, and decreases the patient's perception of the pain.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Accuvein | |
| DEVICE | Routine technique | Placement of peripheral intravenous catheters using the routine technique |
Timeline
- Start date
- 2013-11-01
- Primary completion
- 2017-05-01
- Completion
- 2017-05-01
- First posted
- 2013-12-19
- Last updated
- 2017-05-19
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT02015845. Inclusion in this directory is not an endorsement.