CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 160 enrolled
Drug / intervention
Infrared illuminationdevice
Likely dose
Not stated in record
Key inclusion· 2
  • ✓Children under 2 years old undergoing anesthesia procedures
  • ✓ASA physical status 1, 2, or 3
Key exclusion· 3
  • ✕Emergency procedures requiring anesthesia
  • ✕ASA physical status 4
  • ✕Patients with pre-existing IV access

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

Search/NCT03181542
NCT03181542N/ACompleted
CompareCT.gov

A Randomized Controlled Study of Efficacy of Infra Red Vein Illumination Versus Standard Technique

Milton S. Hershey Medical Center·interventional·Posted Jun 8, 2017·Updated Dec 21, 2021

In Brief

A clinical study evaluating Infrared illumination for Difficult Intravenous Access. Completed, enrolled 160 participants across 1 site.

Detailed Summary

The objective of the study is to assess the efficacy of the vein visualization device AccuVein (AccuVein, Inc., Huntington, NY) in comparison to a standard technique for establishing intravenous (iv) access in the infant and toddler population (\<2years)

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDifficult Intravenous Access
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedJun 8, 2017
Enrollment StartJul 10, 2017
Primary CompletionOct 29, 2020
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 9.1 years ago

Interventions

Infrared illuminationdevice

Infrared illumination of veins using the FDA approved AccuVein (AccuVein, Inc., Huntington, NY) device.