Clinical Trials Logo

Ultrasonography clinical trials

View clinical trials related to Ultrasonography.

Filter by:

NCT ID: NCT03075488 Completed - Obesity Clinical Trials

Ultrasound Prescan vs Conventional Landmark-guided Technique in Spinal Anesthesia in Orthopedic Obese Patients

Start date: March 31, 2017
Phase: N/A
Study type: Interventional

The study is aimed at evaluating whether ultrasound pre-procedural scan with Accuro may reduce needle redirections when performing spinal injection in patients with BMI = or > 30 in orthopedic surgery

NCT ID: NCT02801058 Completed - Ultrasonography Clinical Trials

Ultrasound Evaluation of Changes in Diaphragm Induced by Osteopathic Manipulative Techniques

Start date: September 2015
Phase: N/A
Study type: Interventional

A wide number of osteopathic techniques focusing on diaphragm have been proposed but, although systematically and efficiently used, there is a general lack of evidences able to clarify how and to which extent osteopathic manipulative treatment (OMT) on diaphragm is effective and determines a modification in muscles contractility and motion as well as an objective determination of the benefit on the patients receiving treatment. This study therefore aims at investigating whether, and how, a single session of selected osteopathic diaphragmatic techniques are able to affect muscle motility and thickness, assessed by ultrasounds, in a sample of healthy subjects and to compare results versus a group receiving a sham therapy and another one of non-treated subjects.

NCT ID: NCT02741453 Completed - Critical Care Clinical Trials

Bilateral Internal Jugular Veins Ultrasound Scanning Prior to CVC Placement

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

Central venous catheter placement is a common procedure in the intensive care unit and is a required skill for all residents working in the critical care setting. Central venous catheters (CVC) are placed for a variety of reasons including administration of caustic medications, administration of fluids or blood products for rapid resuscitation, access for hemodynamic monitoring or transvenous pacing, temporary vascular access for dialysis, or inability to obtain peripheral IV access. CVC's are routinely placed in the internal jugular vein in the Vanderbilt medical ICU and ultrasound guidance is used. Placement of the CVC on the right IJ instead of the left IJ is commonly preferred due to the more direct path to the superior vena cava. However, placement in the left IJ may be necessary for a variety of reasons. The investigators intend to compare the standard practice of residents and nurse practitioners placing IJ CVCs in the medical ICU against mandatory screening of the right and left IJ prior to selection of the CVC placement site. The investigators will accomplish this by assessing the relative first pass stick and overall success rates, the rate of aborted procedures, and the rate of complications between standard practice and mandatory screening of bilateral internal jugular veins prior to CVC site selection.

NCT ID: NCT02535013 Completed - Ultrasonography Clinical Trials

Intraoperative Lung Ultrasound in Pediatric Patients

LUS
Start date: August 2015
Phase: N/A
Study type: Interventional

Investigators hypothesized that perioperative lung ultrasound would be beneficial in pediatric patients undergoing cardiac surgery compared to those who did not receive lung ultrasound.

NCT ID: NCT02304133 Completed - Ultrasonography Clinical Trials

Transfer From a Point-of-care Ultrasound Course

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

This study explores the effect of a four-hour ultrasound course on physicians' point-of-care ultrasound performance on patients representing acute abdominal surgical conditions.

NCT ID: NCT02022839 Completed - Ultrasonography Clinical Trials

Role of Lung Ultrasound in Predicting Weaning Outcomes

Start date: December 2010
Phase: N/A
Study type: Observational [Patient Registry]

We aimed to verify the potencial role of bedside lung ultrasound findings of critically ill patients candidates to liberation from mechanical ventilation in predicting weaning outcomes. The analysis will be taken in two times: immediately before and at the and spontaneous breathing trial.

NCT ID: NCT01789801 Completed - Ultrasonography Clinical Trials

A Randomized Study Evaluating the Role of Ultra-sound Guidance When Drawing Radial Arterial Blood Samples

ECHO-PARDIF
Start date: February 21, 2014
Phase: N/A
Study type: Interventional

Previous studies have demonstrated that an experienced ultrasound operator is able to efficiently perform radial arterial puncture on patients where an initial operator failed to puncture arteries via simple palpation. The objective of this study is to compare "difficult-to-puncture" patients randomized into two groups: one group where ultrasound is used to aid artery localisation, and one group where only palpation is used.

NCT ID: NCT01688271 Completed - Pain Management Clinical Trials

Simulation-Based Training for Ultrasound-Guided Perineural Catheter Insertion

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

This study will determine the efficacy of a teaching program incorporating hybrid simulation in training practicing anesthesiologists on ultrasound (US)-guided continuous peripheral nerve block (CPNB). This study will also examine the extent of practice change following participation in a regional anesthesia teaching program incorporating hybrid simulation. In addition, this study will assess remaining obstacles to incorporating the use of US-guided perineural catheters through identifying potential future interventions and "tool-kits" for setting up perineural catheter programs.

NCT ID: NCT01219257 Completed - Ultrasonography Clinical Trials

Longitudinal ULtrasonographic Study of Patients With Spondylarthritis Starting Biological Therapy

ULSPABIT
Start date: September 2011
Phase:
Study type: Observational

Patients with spondylarthritis (SpA) (including ankylosing spondylitis, psoriatic arthritis, arthritis as part of inflammatory bowel disease and reactive arthritis) have axial involvement (the spine) as well as peripheral inflammation in joints and entheses (where the tendons and ligaments are anchored to the bone). Patients with high disease activity of SpA may need biological treatment (anti-TNF alpha), which are very expensive medications. Thus it is necessary to have a sensitive method for assessing the response to treatment. Ultrasonography (US) is a validated and reliable method for assessing disease activity in joints and tendons, and may be used to follow the treatment response. The present study will include patients with SpA starting on anti-TNF alpha treatment (as first biologic medication or when switching to a new biologic treatment). The study is an extension of the ongoing NORDMARD study (Norwegian longitudinal observational study of arthritic patients starting disease-modifying treatment). The patients will be examined by use of US of 38 joints and 14 entheses at baseline and after 3, 6 and 12 months. The objectives are to explore US as a method to assess peripheral inflammatory activity for evaluation of response to medication as well as to compare the US pathology with clinical and laboratory findings.

NCT ID: NCT01189188 Completed - Ultrasonography Clinical Trials

Ultrasound Guidance for Radial Arterial Blood Sampling

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

The investigators aim to determine if ultrasound guidance results in improved technique when drawing blood via a radial artery puncture.