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Ultrasound clinical trials

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NCT ID: NCT03164369 Completed - Ultrasound Clinical Trials

Real Time 3D Navigation and Traditional US to Identify Epidural Space Depth in Pregnancy

Accuro
Start date: April 1, 2017
Phase: N/A
Study type: Observational

The aim of this double blinded study is to assess the abilities of the SpineNav3DTM technology (Accuro) to identify the lumbar epidural space in parturients using as comparator a standar ultrasound (US) device.

NCT ID: NCT03135379 Completed - Ultrasound Clinical Trials

Comparison of Patient Satisfaction Using Heated Versus Room Temperature Ultrasound Gel

HUGS
Start date: April 2016
Phase: N/A
Study type: Interventional

The purpose of this single-blind, randomized control trial will be to investigate whether simply having warmed gel, as compared to room-temperature gel, during a bedside ultrasound significantly improves patient satisfaction scores.

NCT ID: NCT02661607 Completed - Critical Care Clinical Trials

Point of Care Echocardiography Versus Chest Radiography for the Assessment of Central Venous Catheter Placement

Start date: October 2014
Phase: N/A
Study type: Interventional

A prospective study to compare the use of point of care echocardiography versus routine chest radiography for the assessment of central venous catheter placement.

NCT ID: NCT02333786 Completed - Child Clinical Trials

Ultrasound-guided Arterial Catheterization in Pediatric Patients

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

Investigators designed a prospective randomized controlled study to compare the long-axis/in-plane and short-axis/out-of-plane methods during the ultrasound-guided arterial catheterization in pediatric patients younger than 5 years old.

NCT ID: NCT02062567 Completed - Ultrasound Clinical Trials

Ultrasonographic Guided Treatment of Acute Achilles Tendon Rupture. Evaluation of Two Novel Ultrasonographic Measurements

Start date: February 2014
Phase: N/A
Study type: Observational

With this project the investigators wish to: 1. Test the reproducibility of Amlang's ultrasound classification by examining the intra- and inter-rater reliability. 2. Investigate whether Amlang's ultrasound classification is able to predict which patients are likely to develop complications when treated non-operatively. 3. Investigate whether Barfod's length measurement is able to predict which patients are likely to develop complications when treated non-operatively.

NCT ID: NCT01699373 Completed - Ultrasound Clinical Trials

A Trial on Ultrasound-assisted Spinal Anaesthesia

Start date: April 2011
Phase: N/A
Study type: Interventional

A randomised controlled trial comparing the use of pre-procedural ultrasound scanning with manual palpation to identify landmarks for performance of spinal anaesthesia.

NCT ID: NCT01666626 Completed - Crohn's Disease Clinical Trials

Ultrasound Stiffness Imaging in Crohn's Disease

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

The purpose of this study is to determine whether ultrasound-based assessment of intestinal stiffness in patients with Crohn's disease predicts the effectiveness of medical therapy or the need for surgical resection.

NCT ID: NCT01519167 Completed - Ultrasound Clinical Trials

Open-Label, Safety Study Evaluating the Use of Dexmedetomidine in Pediatric Subjects Undergoing Procedure-Type Sedation

Start date: October 2012
Phase: Phase 4
Study type: Interventional

The objective of this study is to evaluate the safety of dexmedetomidine in a pediatric population requiring non-intubated, spontaneous breathing, moderate to deep sedation (NI-MDS) for elective diagnostic or therapeutic procedures, expected to take more than 30 minutes.

NCT ID: NCT00872703 Completed - Ultrasound Clinical Trials

Does Normal Brain Imaging Predict Normal Neurodevelopmental Outcome in Fetuses With Proven Cytomegalovirus Infection?

Start date: January 2008
Phase: N/A
Study type: Observational

Cytomegalovirus (CMV) is the largest member of the virus family Herpesviridae that infects almost all humans at some point in their lives (Ross, 2004). Congenital CMV infection is most likely to occur when the mother experiences a primary infection during pregnancy, and it is much less common in cases of reactivation of the disease or infection by a different CMV strain (Boppana 1999, Endres 2001). The prevalence of congenital CMV infection varies between 0.15-2.2% (Ross 2004, Ross 2006, Malm 2007). While most infants born with congenital CMV infection are asymptomatic, 10 to 15% show clinical findings at birth (Ross 2004). It is generally agreed that congenital CMV infection, whether it is symptomatic or not, is a major risk factor for perceptual deficits. However, its influence on children's future neuropsychological functioning is less well established. Symptomatic congenital CMV infection is a major risk factor for poor developmental outcome (Williamson 1982, Kylat 2006, Dollard 2007), but the available data regarding neuropsychological outcome for asymptomatic children is extremely diverse (Conboy 1986, Ivarson 1997, Kashdan 1998, Temple 2000, Zhang 2007). We evaluated the neuropsychological outcome of children with congenital cytomegalovirus (CMV) infection and normal consecutive fetal neurosonographic examinations and determined whether Magnetic Resonance Imaging (MRI) provided additional information in these cases.