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Radiography clinical trials

View clinical trials related to Radiography.

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NCT ID: NCT05176886 Completed - Clinical trials for Central Venous Catheter

Correct Tip Position of Central Venous Catheters

Start date: July 8, 2018
Phase:
Study type: Observational

Patients, ages between 18-70 years, who require central venous catheter will be enrolled for the study. Central venous catheter will be inserted using patient's height formula by Seldinger technique. Anterioposterior chest radiography will be used to assess the correct tip position. Catheters that are below the carina more than 1 cm, will be pulled back for repositioning. Catheters that are above the carina more than 1 cm, will be changed by another catheter. The investigators aim to evaluate the formula for correct tip positioning for central venous catheters

NCT ID: NCT05076188 Completed - Emergencies Clinical Trials

PARamedical Abnormalties Detection of Traumatic Bone Lesion of the extremitIeS

PARADIS_1
Start date: March 1, 2021
Phase:
Study type: Observational

This study assesses the performance of radiographers in detecting radiological anomalies of the appendicular skeleton in emergency department. This is a retrospective study comparing the radiographers' diagnostic performance before and after dedicated training, assisted or not by artificial intelligence software. All performances will be evaluated and compared.

NCT ID: NCT04481711 Completed - Orthopedic Disorder Clinical Trials

Total Knee Arthroplasty and Clinical Findings

Start date: November 8, 2018
Phase: N/A
Study type: Interventional

Knee osteoarthritis is a common disease that causes pain and loss of function. Total Knee Arthroplasty (TKA) is a frequently used surgical method in the treatment of severe knee osteoarthritis. The aim of this study was to investigate the effect of TKA on IL-6, TNF-α and IL-1β cytokine levels, pain intensity at rest and walking, knee joint valgity angle,malaligment, functional status and knee joint position sense.

NCT ID: NCT03876379 Completed - Orthopedic Surgery Clinical Trials

Brain Power Spectral Density Under Propofol

PROBRAIN
Start date: January 24, 2015
Phase:
Study type: Observational [Patient Registry]

In the operating room, the state of anesthesia is monitored during general anesthesia-induced hypnosis through EEG-based neuro-monitoring. Recent studies suggest that variables extracted from per-operative EEG change as brain ages. Furthermore, aging is itself an independant factor associated to an increased sensitivity to General Anesthesia (GA). Among fragility sign, per-operative Burst Suppression (BS) has been associated to a poor postoperative cognitive trajectory. The main goal of this observational clinical study is to extend the traditional use of per-operative EEG to the detection and prediction of various degrees of brain fragility, depending on the depth of anesthesia (DoA).

NCT ID: NCT03853226 Completed - Radiography Clinical Trials

Rational for the Use of Velocity-Pressure Loop in the Operating Room

VPLOOP
Start date: January 5, 2014
Phase:
Study type: Observational

In surgical patients considered with "high cardiovascular risk", by their field or by the nature of their intervention, it is recommended to use hemodynamic monitoring including a continuous measurement device of arterial pressure and cardiac output (CO). However, targeting mean arterial pressure (MAP) with boluses of selective peripheral vasopressors (without positive inotropic or chronotropic effects) could have deleterious effects on CO. Thus, it seems important to use a combined analysis of MAP and CO to estimate the afterload-related cardiac performance (ACP) The investigators recently proposed a cardiac afterload monitoring, in the descending thoracic aorta, based on a combined analysis of flow velocity signal recorded by trans-oesophageal Doppler and aortic pressure, the Velocity-Pressure Loop (VP Loop). VP Loop, and its derived indicators, especially Global AfterLoad Angle (GALA), could be useful during hemodynamic management for continuous cardiac afterload monitoring. However, in cardiology unit, cardiac afterload is usually measured at the ascending aorta behind the aortic valves. The main objective of this study is to compare VP Loop parameters build in the ascending and descending thoracic aorta according to patient cardiovascular risk factors.

NCT ID: NCT03769142 Completed - Radiography Clinical Trials

Cerebral Perfusion During Induction of General Anesthesia

Start date: February 1, 2014
Phase:
Study type: Observational

Arterial hypotension during general anesthesia remains a factor of poor outcomes, increases the risk of myocardial infarction, acute kidney injury and 1-year mortality. Furthermore, arterial hypotension may also decrease cerebral perfusion contributing to worsen neurological outcome. It seems necessary to monitor cerebral perfusion during anesthesia and to define individual dynamic targets of blood pressure. The goal of this study is to evaluate cerebral perfusion change in adult patients with or without cardiovascular risk factors during a standardized propofol-remifentanil anesthesia induction. Cerebral perfusion will be evaluated and compared using the simultaneously measure of TCD, NIRS and BIS. Those measures will be also repeated during and after treatment of arterial hypotension episodes in both groups.

NCT ID: NCT03756935 Completed - Radiography Clinical Trials

Early Detection of Intra Operative Hypotension (IOH) During the Induction of General Anaesthesia

Start date: November 1, 2014
Phase:
Study type: Observational

During general anaesthesia, intraoperative hypotension (IOH), defined as a mean arterial pressure (MAP) drop of more than 20%, is frequent with potential deleterious effects for patients. Pulse oximeter is mandatory in the operating room making photoplethysmographic (PPG) signal and parameters such as the relative dicrotic notch height (Dicpleth) or the perfusion index (PI) readily available. The purpose of this study is to investigate whether Dicpleth and PI could detect IOH during anaesthesia induction and follow their variations during vasopressor boluses.

NCT ID: NCT02925936 Completed - Radiography Clinical Trials

Choice of Tube Extremity in Emission of Lowest Radiation Dose in Pediatric Patients

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

Compare the radiation in pediatric patients thyroid submitted to chest X-ray using the position of the anode and cathode.