Trials / Terminated
TerminatedNCT05204082
A Study to Evaluate SU-VEID™ for Improving Peripheral Venous Access Success in Children
Use of SU-VEID™ As An Adjunct to Vein Visualization Technology to Improve Peripheral Venous Access Success in Children
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 169 (actual)
- Sponsor
- Mayo Clinic · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to determine if use of the SU-VEID™ in children facilitates an increase success rate of peripheral intravenous starts, in comparison to the conventional method of vein entry techniques.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Single Use Vein Entry Indicator Device | Electronic pressure sensing device, integrated to a conventional needle catheter, and which indicates continuously during intravenous cannulation whether the tip of the needle is inside or outside of a vein, to assist a clinician in intravenous cannulation. |
Timeline
- Start date
- 2022-03-28
- Primary completion
- 2022-07-21
- Completion
- 2022-07-21
- First posted
- 2022-01-24
- Last updated
- 2024-05-23
- Results posted
- 2024-05-23
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05204082. Inclusion in this directory is not an endorsement.