Status:
COMPLETED
A Comparison of the First Attempt Success Rate of Cannulation Between the Accuvein Apparatus and Standard Technique
Lead Sponsor:
American University of Beirut Medical Center
Conditions:
Procedural Complication
Eligibility:
All Genders
Up to 18 years
Phase:
NA
Brief Summary
Background: The AccuVein AV300 device helps in venepuncture and intravenous (IV) cannulation. It uses infrared light that can be absorbed by the blood hemoglobin so that veins location is clearly view...
Detailed Description
Patients who fulfilled the inclusion criteria and provided informed consent were assigned to one of two groups using a randomization program that assigned research participants into group A (AccuVein ...
Eligibility Criteria
Inclusion
- Patients less than 18 years of age, American Society of Anesthesiologist Physical Status (ASA) status I, II or III, undergoing elective surgery or examination under anesthesia, which did not have existing intravenous access.
Exclusion
- Existing intravenous access, malformations or infections at the potential site of insertion, need for emergency surgery, and inability or unwillingness of parent or legal guardian to give written informed consent.
Key Trial Info
Start Date :
February 10 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 10 2014
Estimated Enrollment :
184 Patients enrolled
Trial Details
Trial ID
NCT03462745
Start Date
February 10 2013
End Date
February 10 2014
Last Update
February 26 2019
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