Clinical Trials Logo

Ultrasound clinical trials

View clinical trials related to Ultrasound.

Filter by:

NCT ID: NCT03425162 Completed - Postoperative Pain Clinical Trials

Ultrasound Guided Anterior Quadratus Lumborum Block

Start date: February 12, 2018
Phase: N/A
Study type: Interventional

Percutaneous nephrolithotomy (PNL) is frequently used today for renal stones. percutaneous nephrolithotomy (PNL) procedure has become the treatment of choice for many patients with symptomatic renal stones . Patients undergoing PNL suffer from acute postoperative pain, despite a multimodal analgesic regime. This is a randomised controlled trial efficacy of the anterior Quadratus Lumborum Block (QLB) in terms of analgesic efficacy in patients who undergo percutaneous nephrolithotomy.

NCT ID: NCT03416608 Completed - Ultrasound Clinical Trials

Patient Experiences of Use of Point-of-Care Ultrasound in General Practice

Start date: January 15, 2018
Phase:
Study type: Observational

This study in part of a larger cohort study (clinical trials ID number: NCT03375333) that examine the use of ultrasound in general practice. In the present study patient experiences, with use of ultrasound in the consultation at the general practitioners office, will be explored through a questionnaire.

NCT ID: NCT03375333 Completed - Ultrasound Clinical Trials

How Point-of-Care Ultrasound Affects the Diagnostic Process in General Practice.

Start date: January 15, 2018
Phase:
Study type: Observational

This study explores how Point of Care Ultrasound (POC-US) is used in general practice in Denmark and how it affects the diagnostic process and treatment of patients. Twenty general practitioners (GPs) will register information each time they use POC-US during a one month period. The information will include indications and frequencies of the performed POC-US examinations, change in tentative diagnosis, plan, and treatment before and after the use of POC-US in relation to confidence in the tentative diagnosis, findings and quality of the POC-US examination. This is an observational study without any intervention.

NCT ID: NCT03277599 Completed - Pain Management Clinical Trials

Comparison of Two Pain-treatment Techniques After Tympanomastoid Surgery Pain

Start date: July 5, 2016
Phase: N/A
Study type: Interventional

Analgesia following tympanomastoid surgery is critical for the prevention of postoperative . There are very few regional anesthesia methods used to achieve this goal.

NCT ID: NCT03276364 Completed - Shock Clinical Trials

The Impact of Point-of-Care Ultrasound

Start date: July 21, 2014
Phase: N/A
Study type: Observational

Point-of-care ultrasound (POCUS) has been found to be useful for aiding in the prediction of fluid responsiveness. It is unknown if trainees can effectively utilize this tool to improve their assessment of fluid responsiveness. In this prospective, observational study, pulmonary and critical care fellows are asked to make 2 assessments of fluid responsiveness in adults with shock: (1) based on clinical exam alone (Clinical) and (2) after performing a POCUS (Clinical + US). The accuracy of their pre- and post-ultrasound assessments are compared using a bioreactance monitor and passive leg raise test as the gold standard of fluid responsiveness in this study.

NCT ID: NCT03212248 Completed - Clinical trials for Community-acquired Pneumonia

CRP and Thoracic Emergency Ultrasound in Pneumonia

TUS-STRAT
Start date: January 2, 2016
Phase: N/A
Study type: Observational

This preliminary study investigates in patients with possible clinical diagnosis of pneumonia, clues and biomarker assessed at Emergency Department (ED) triage, potentially predicting detection of lung consolidation by Thoracic-ultrasound (TUS) and/or by Chest-X-Rays. Cough and high admission CRP levels will be defined according to the cutoff defined by ROC analysis, will be challenged if independently associated with TUS lung consolidation detection High level of the chosen biomarker, and any of the considered symptoms, in otherwise not extremely critical patients (CURB65≤3), should prompt to immediate confirm by TUS, during the physical examination. This may limit the need of further radiological investigations allowing targeted workup.

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: NCT03160222 Active, not recruiting - Body Composition Clinical Trials

Validation of Bedside Ultrasound to Predict Body Composition in Non- and Critically Ill Patients

USVALID
Start date: January 2017
Phase: N/A
Study type: Interventional

The prospective study will include 200 patients and 50 critically ill patients, who had an abdominal computed tomography (CT) scan including the L3 level for any clinical reason. Ultrasound scans of the anterior thighs and forearms will be taken after the CT scan within 48 hours. Bioelectrical impedance analysis (BIA) will also be performed. In addition muscle strength, mobility, physical function and nutrition will be assessed. Primary outcome is the prediction of CT-based whole body muscle and fat volume and BIA-based fat and lean body mass from ultrasound-based muscle and fat thickness. Other secondary outcomes include the intra- and interrater reliability of the CT evaluation and ultrasound examination of muscle and fat mass. The relationship between clinical aspects (strength, mobility, physical function, nutrition) and whole body composition is another secondary outcome.

NCT ID: NCT03142906 Recruiting - Surgery Clinical Trials

Perioperative Point-of-Care Ultrasound

POCUS-RCT
Start date: April 4, 2017
Phase: N/A
Study type: Interventional

The goal of this study is to assess the impact of perioperative point-of-care ultrasound (POCUS) assessment on patient-important outcomes (e.g. hospital length of stay, length of stay in recovery, mortality etc.) and perioperative patient management strategies, in patients undergoing non-elective non-cardiac surgeries.

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.