Evaluation of Accuvein in Adult Patients
Phase 4
Terminated
- Conditions
- Catheterization
- Interventions
- Device: Accuvein
- Registration Number
- NCT01020461
- Lead Sponsor
- Hopital Foch
- Brief 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 522
Inclusion Criteria
- adults requiring a venous blood sampling or the placement of a venous peripheral catheter
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Exclusion Criteria
- none
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Peripheral IV catheter placement Accuvein To use Accuvein to improve the effectiveness of placing peripheral IV catheter Venous blood sampling Accuvein To use Accuvein to improve the effectiveness of venous blood sampling
- Primary Outcome Measures
Name Time Method Time to successful blood sampling or to successful placement of IV catheter one hour
- Secondary Outcome Measures
Name Time Method Pain Immediately after attempts Number of attempts required Immediately after attempts Increases in the ease and efficiency of venous cannulation perceived by the operator) Immediately after attempts
Trial Locations
- Locations (1)
Hôpital Foch
🇫🇷Suresnes, France