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N/A N=749 Randomized Single-blind Treatment

Ultrasound-image Guided Versus Doppler Guided Versus Palpation Technique for Arterial Cannulation in Adults

Anesthesia

Enrolled (actual)
749
Serious AEs
0.0%
Results posted
Jun 2017
Primary outcome: Primary: First Attempt Success Rate With 3 Different Technique — 132; 101; 96 participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Ultrasound (Procedure); Doppler (Procedure); Palpation (Procedure)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Iowa
Primary completion
Dec 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
First Attempt Success Rate With 3 Different Technique
132; 101; 96
SECONDARY
Time to Successful Cannulation
32; 118; 91
SECONDARY
Total Success Rate
170; 147; 160

Summary

Radial arterial cannulation is a common invasive procedure for real-time measurement of arterial blood pressure. Placement of the arterial catheter using conventional palpation is often relatively easy and quick, but this is not always true. A relatively new method for direct visualization of the artery is the use of two-dimensional ultrasound. This technique allows cannulation of the artery to take place under real-time visualization and may increase the success rate of first time pass of the needle. Another technique utilizing Doppler has also proven to be effective in cannulating the radial artery. This technique utilizes changes in acoustic pitch as the probe passes directly over the artery. The primary objective of this study is to compare the first attempt success rate for radial artery cannulation among the palpation, Doppler and U/S guided technique when applied by trainees. Secondary outcomes include: success rate within 5 minutes, successful, number of attempts required, and correlation between success rate and operator experience for successful cannulation of the radial artery.

Eligibility Criteria

Inclusion Criteria

  • Main OR patients at UIHC who require arterial catheter placement for surgery

Exclusion Criteria

  • The patients who will be excluded from the study include those who have had arterial cannulation in the previous month, infections at site of insertion, and AV shunts in upper extremity.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01276171). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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