Geneva, Aug. 6 -- International Clinical Trials Registry received information related to the study (ACTRN12626000915358) titled 'Feasibility of First Pass Cannulation Success Rate in Peripheral Intravenous Cannulation on Adults Using a Novel Ultrasound Device' on July 24.
Study Type: Interventional
Study Design:
Purpose: Treatment
Allocation: Non-randomised trial
Masking: Open (masking not used)
Assignment: Single group
Type of endpoint: Efficacy
Primary Sponsor: VeinTech Pty Ltd
Condition:
Peripheral intravenous access
Peripheral intravenous access
Anaesthesiology - Other anaesthesiology
Public Health - Health service research
Intervention:
This study aims to evaluate the usability and clinical effectiveness of the VeinWise devic...