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Catheterization clinical trials

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NCT ID: NCT03582540 Completed - Catheterization Clinical Trials

Early Versus Delayed Double-guidewire Technique in Difficult Biliary Cannulation. (DFG)

DFG
Start date: November 2, 2016
Phase: N/A
Study type: Interventional

This is a prospective randomized comparative multicentric study. Briefly, we will analyze the technical success, performance and clinical outcomes of early versus delayed double-guidewire technique (DGT) in difficult biliary cannulation.

NCT ID: NCT03565419 Completed - Ultrasonography Clinical Trials

Use of Smart Glasses for Ultrasound Guided Peripheral Venous Access

Start date: June 20, 2018
Phase: N/A
Study type: Interventional

Investigators aimed to explore the feasibility of smart glasses connected to a wireless ultrasound transducer for the peripheral venous access. Residents who have basic skills of ultrasound guided procedure participate in the simulation. Each participant plays the following two roles for ultrasound guided peripheral venous access; ultrasound guided peripheral venous access with and without wearing smart glasses. The order of performing two roles is determined by a randomized process and the gap between two roles are five days. The primary outcome is the time of successful blood aspiration, and secondary outcomes are first time success rate, the number of skin puncture, the number of needle redirection, the number of head movement, and subjective difficulty.

NCT ID: NCT03405623 Completed - Ultrasonography Clinical Trials

Dynamic SAX vs Conventional LAX in Radial Artery Cannulation.

Start date: January 30, 2018
Phase: N/A
Study type: Interventional

When performing vascular cannulation such as radial artery cannulation, ultrasonography (US) helps proper positioning of the tip of needle in the vascular lumen, which facilitating cannulation of the catheter and successful pressure monitoring. Conventionally, short-axis out-of-plane (SAX) and long-axis in-plane (LAX) views are commonly used method to image the target vessel during cannulation under US guidance. Dynamic needle tip positioning (DNTP) method is newly introduced by one group of investigators who conducted a related study using vascular phantom model. In DNTP, SAX is used, and additionally, when the needle tip is imaged in the screen as an echogenic point, the practitioner (a) proximally moves the US probe a bit, and then (b) the needle is advanced until the needle tip reappears in the screen. In this manner, the practitioner repeats (a) and (b) until the needle is inserted 1 cm into the lumen of vessel, and then the catheter is inserted to finish the procedure. DNTP has not been compared to conventional imaging methods. The aim of this trial is to see the effect of DNTP on success rate of the radial artery cannulation at the first attempt, compared to the conventional LAX.

NCT ID: NCT03254303 Completed - Catheterization Clinical Trials

Intravenous Cannulation In Children During Sevoflurane Induction

Start date: August 1, 2016
Phase: N/A
Study type: Interventional

This interventional simple-blind,randomized trial has included 90 children of American Society of Anesthesiologist (ASA) physical status I or II aged between 1 to 12 years of either sex, scheduled for for outpatient minor surgery under general anesthesia. This study examined whether one should make iv attempts during the early induction period (at 60 seconds) or lately (90 or 120 s) and waiting until the child receives additional sevoflurane inhalation anesthesia.

NCT ID: NCT02899546 Completed - Infection Clinical Trials

Study of Peripherally Inserted Central Catheter (PICC)-Related Infections in a Tropical Area

Septi-PICC
Start date: November 1, 2015
Phase:
Study type: Observational

Septi-PICC study aims at assessing incidence of Peripherally Inserted Central Catheter (PICC)-related infections among patients managed in the University Hospital of La Reunion for PICC setting.

NCT ID: NCT02431858 Completed - Nerve Block Clinical Trials

Catheter Over Needle vs Catheter Through Needle

Start date: May 2015
Phase: Phase 4
Study type: Interventional

To randomize 108 patients undergoing knee replacement surgery to catheter through needle or catheter over needle femoral nerve blocks, then monitor the catheters for leakage to see if there is a difference.

NCT ID: NCT01479153 Completed - Critical Care Clinical Trials

Venous Site for Central Catheterization

3SITES
Start date: October 2011
Phase: N/A
Study type: Interventional

Central venous catheters are needed in the critical care setting to administer drugs. Three sites are available to gain vascular access: subclavian, internal jugular and femoral. Each site has complications, but there is no randomized controlled study which compared the 3 sites. The investigators hypothesis is that subclavian catheterization reduces the risk of major complications compared to internal jugular or femoral.

NCT ID: NCT01347463 Completed - Catheterization Clinical Trials

Validation of the Ipsilateral Nipple as the Directional Guide for Internal Jugular Vein (IJV) Catheterization

Start date: June 2011
Phase:
Study type: Observational

Traditional teaching that suggests the ipsilateral nipple as the directional guide for needle advancement during Internal Jugular Vein (IJV) catheterization has weak grounds. The investigators attempt to validate this long-standing statement.

NCT ID: NCT01133652 Completed - Catheterization Clinical Trials

Variation In Success of Intravenous (IV) Placement With Observation Using New Techniques

VISION
Start date: May 2010
Phase: Phase 4
Study type: Interventional

Children fear having an intravenous (IV) needle placed because of the pain that they will experience. The more needle punctures that a child has to endure before the IV is successfully placed, the greater the pain experienced and anxiety suffered. In addition, false starts increase the demands on medical staff and can increase the length of the emergency department stay. Often, veins are difficult to see or feel, particularly in an unwell, dehydrated child or in young infants who have more fat below the skin surface. Also, the venous pattern below the skin surface naturally varies from person to person and therefore success in placing IVs leaves room for improvement. Technology may be able to play an important role is improving the rates of success. The investigators wish to investigate whether the use of either an Ultrasound machine or a VeinViewer machine can improve the rate of success of the initial attempt (skin puncture) at peripheral IV placement in comparison to the current standard approach.

NCT ID: NCT00903825 Completed - Catheterization Clinical Trials

Duplex Guided Application of Local Anesthetic Before Femoral Artery Catheterization

Start date: January 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this study is to evaluate the optimization of local anesthetic effect with duplex ultrasound-guided injection of lidocaine before femoral artery puncture during diagnostic or therapeutic interventional procedures. In total, 200 patients scheduled for various diagnostic or therapeutic interventional radiology procedures requiring femoral artery puncture, will be randomized in two groups after informed consent. Patients will be randomized to undergo groin local anesthesia with the proposed method of duplex ultrasound guided injection of lidocaine versus standard injection of lidocaine with manual palpation (control group). The protocol includes the registration of patients' demographics (age, gender, risk factors for peripheral arterial disease), arterial morphological characteristics (calcifications and presence of atheromatous disease), as well as technical details of the procedure (total puncture duration, sheath size, antegrade/retrograde puncture, etc.) Primary study endpoint will be peri-procedural pain that will be assessed with the use of a visual analog scale (VAS) completed by the patient at the end of the procedure. Secondary study endpoints will evaluate procedural safety and complications during the immediate post-procedural period (up to 7 days).