CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 184 enrolled
Drug / intervention
AccuVein AV 300device
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03462745
NCT03462745N/ACompleted

Randomized Cross Over Study Comparing the First Attempt Success Rate of Intravenous Cannulation in Children Using the AccuVein AV 300 Apparatus Versus the Standard Technique

American University of Beirut Medical Center·interventional·Posted Mar 13, 2018·Updated Feb 26, 2019

In Brief

A clinical study evaluating AccuVein AV 300 for Procedural Complication. Completed, enrolled 184 participants.

Detailed 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 viewed on the skin's surface. Objectives: To assess the effectiveness of the AV300 device over the standard technique in increasing the first-time success rate (SR) for pediatric patients who needed IV cannulation. Methods: This was a prospective cross study of patients aged 0-18 years scheduled for surgery or examination under anesthesia but without having an existing IV access and after providing consent form. Patients were randomized into two groups; cannulation with AV300 or standard insertion performed by experienced pediatric anesthesiologists and residents under training.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
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Timeline

N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedMar 13, 2018
Enrollment StartFeb 10, 2013
Primary CompletionFeb 10, 2014
TodayJul 2, 2026
Enrollment to primary: 1 yearPosted 8.3 years ago

Interventions

AccuVein AV 300device

Assess the effectiveness of the AccuVein AV300 device over the standard technique in increasing the first-time success rate (SR) for pediatric patients who needed IV cannulation