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Cannulation clinical trials

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NCT ID: NCT06271499 Completed - Catheterization Clinical Trials

The Effect of Using Smart Glasses Integrated Ultrasonography on Radial Artery Catheterization

Start date: August 1, 2022
Phase: N/A
Study type: Interventional

The use of Ultrasonography (USG) in arterial catheterization, in which the comfort of the practitioner and hand-eye coordination become very important, is frequently needed by anesthesiologists in their daily practice. The aim of this study is to evaluate the success rate and anesthesiologist's satisfaction between two practitioners with different levels of experience in radial artery catheterization with smart glasses USG.

NCT ID: NCT05139212 Completed - Dexmedetomidine Clinical Trials

Determination of Optimum Time for Intravenous Cannulation in Children With Dexmedetomidine Premedication

Start date: December 2, 2021
Phase:
Study type: Observational

Inhalational induction with sevoflurane, nitrous oxide, and oxygen is accepted as a safe technique to avoid any movement during intravenous cannulation in children. In addition, intranasal dexmedetomidine could be used for premedication to reduce preoperative anxiety in preschool children. Early attempts to place, an intravenous line may result in movement and respiratory complications like coughing or laryngospasm. On the other hand delay in cannulation may prevent effective management of bradycardia and hypotension. There are a number of studies examining the optimum time for cannulation after sevoflurane induction. However, it is not known whether the addition of dexmedetomidine premedication affects the time for intravenous cannulation following induction with sevoflurane and nitrous oxide.

NCT ID: NCT01042613 Completed - Cannulation Clinical Trials

A Comparison of the Success Rate Of Cannulation Between The Accuvein Apparatus And Standard Technique

Start date: January 2010
Phase: N/A
Study type: Interventional

1. This study will compare the first attempt success rate of cannulation in research participants randomized to using a new FDA approved AccuVein AV300 device for intravenous access with research participants randomized to standard cannulation methods. 2. This study will assess if insertion of intravenous cannula is faster when intravenous access is assisted by the AccuVein AV300 device as compared to the standard technique. 3. This study will assess if the number of skin punctures is fewer when intravenous access is assisted by the AccuVein AV300 device as compared to the standard technique.