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Local Anaesthesia clinical trials

View clinical trials related to Local Anaesthesia.

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NCT ID: NCT05108714 Completed - Local Anaesthesia Clinical Trials

Intradermal Lidocaine Via MicronJet600 Microneedle Device

Start date: January 29, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to determine efficiency and safety of injecting a micro-amount of 2% lidocaine with the commercially available microneedle device MinronJet600 (NanoPass Technologies Ltd, Israel) (registration number RZN2017/5544 by Federal Service for Surveillance in Healthcare of Russian Federation) to achieve rapid local anesthesia for peripheral venous cannulation.

NCT ID: NCT05083975 Completed - Local Anaesthesia Clinical Trials

Buzzy System Compared to Topical Anaesthesia During Infiltration Injection in Children.

Start date: July 23, 2022
Phase: N/A
Study type: Interventional

Aim of the study is to test the effect of Buzzy System (vibrating device) compared to topical anaesthesia on pain reduction during injection of infiltration anaesthesia in children.

NCT ID: NCT03445182 Completed - Pain Management Clinical Trials

Effectiveness of DentalVibe in Reducing Injection Pain and Anxiety During Local Anaesthesia in Children

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to determine the effectiveness of DentalVibe (DV) in reducing injection pain and anxiety associated with local anaesthesia in paediatric patients. The clinical trial is a randomized split-mouth assignment. Included patients are 8-12 years old requiring local anesthetic infiltration with conventional syringe (CS) for extraction of two primary maxillary molars bilaterally. Eligible patients undergo two single-visit treatments after CFSS-DS measurement before each, where as DV is allocated to either first or second local anaesthesia procedure. Primary outcome measure will be pain felt during injection, reported by patient on VAS. Secondary outcome measures: self-reported anxiety during injection on FIS; pain-related behavior according to FLACC scale; heart-rate dynamics; patient preference to local anaesthesia method - CS or CS+DV.

NCT ID: NCT02023762 Completed - Clinical trials for Mitral Regurgitation

Deep Sedation Instead of General Anaesthesia in Percutaneous Mitral Valve Repair Using the MitraClip® System

Start date: January 2012
Phase: N/A
Study type: Observational

Percutaneous mitral valve repair (PMVR) with the MitraClip® system has emerged as a therapeutic alternative to surgical valve repair in patients who are at high risk and unsuitable for surgery. The PMVR procedure is typically performed under general anaesthesia, but the MitraClip® is also feasible in deep sedation. The aim of this study is to investigate the safety of deep sedation in patients undergoing the PMVR procedure and to evaluate how deep sedation in comparison to general anaesthesia influences procedural time and in-hospital stay.