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NCT ID: NCT04127630 Completed - MRI Clinical Trials

MRI STUDY OF THE LPEC

Start date: February 1, 2019
Phase:
Study type: Observational

Cricoid pressure is still considered as a standard of care in order to prevent the gastric regurgitation in full stomach surgery1. However, this attitude has been challenged in several case reports as oesophageal rupture, difficult intubation, and even failing to occlude the oesophagus. Moreover, in a large prospective randomized study , this maneuver has failed to show a definite benefit2. The lateral deviation to the left of the oeso deviate to the left side3,4 has led to the description of a new maneuver to compress directly the oesophagus at the low left paratracheal level. This maneuver has been shown to prevent gastric air insuflation during the ventilation. In the present study, the investigators aim to asses with an magnetic resonance imaging the compressibility of the oesophagus.

NCT ID: NCT04126798 Completed - Vestibular Diseases Clinical Trials

2BALANCE: Cognitive-motor Dual-tasking in Persons With Vestibular Disorders

Start date: August 12, 2019
Phase:
Study type: Observational

The overall aim of this study is to elucidate the impact of a vestibular dysfunction on the cognitive and motor performance by means of an extensive test protocol, evaluating the vestibular, cognitive and motor function using single as well as dual-task paradigms.

NCT ID: NCT04126395 Completed - Clinical trials for Autism Spectrum Disorder

An Explorative RVA of the Motor Development of Children With DCD <2y

RVA_DCD
Start date: September 14, 2020
Phase:
Study type: Observational

This study compares motor development in three groups of infants (controls, DCD, DCD+ASD) before the age of 2 years using retrospective video analysis of infants in home video contexts.

NCT ID: NCT04126356 Completed - Laryngoscopy Clinical Trials

VIDEOLARYNGOSCOPY STUDY OF THE LPEC

Start date: February 1, 2019
Phase:
Study type: Observational

Check the intubation conditions during laryngoscopy without external mobilization of the larynx, with Sellick manoeuvre or with low paratracheal esophagal compression.

NCT ID: NCT04125927 Completed - Cystinosis Clinical Trials

Cystadrops in Pediatric Cystinosis Patients From Six Months to Less Than Two Years Old (SCOB2)

SCOB2
Start date: September 1, 2020
Phase: Phase 3
Study type: Interventional

Cystadrops® is currently indicated in adults and children from 2 years of age diagnosed with cystinosis with corneal crystal accumulation observed. However administration of Cystadrops® in patients below 2 years old could be of value for these patients and prevent the crystal deposit. It is the reason why as part of the Cystadrops® pediatric investigational plan (PIP), RECORDATI Rare Diseases committed to conduct a clinical study to assess Cystadrops® safety and efficacy in the pediatric population from 6 months to less than 2 years old.

NCT ID: NCT04124328 Completed - Atrial Fibrillation Clinical Trials

Evaluation of Vein of Marshall Ethanol Infusion During Left Atrial Linear Ablation in Patients With Persistent Atrial Fibrillation

MARSHALINE
Start date: October 15, 2019
Phase: N/A
Study type: Interventional

In this prospective, randomized, controlled, unblinded, mono-center study, we aim to evaluate the efficacy of vein of Marshall ethanol infusion during left atrial linear ablation in patients with atrial fibrillation compared to the ALINE protocol.

NCT ID: NCT04122963 Completed - Atrial Fibrillation Clinical Trials

CLOSE-guided Pulmonary Vein Isolation Using High Power and Stable RF Applications

POWERAF
Start date: February 15, 2019
Phase: N/A
Study type: Interventional

In this prospective, randomised, controlled, unblinded,monocentric study, we aim to evaluate the safety and efficacy of higher power CLOSE-guided PVI in patients referred for a first ablation for paroxysmal AF. We aim to include 100 patients into two groups (1:1). The experimental group will receive AF ablation with 45 Watt and stricter stability criteria (3 mm for 3 seconds) compared to the control group which will receive AF ablation according to the standard CLOSE-protocol (35 Watt and stability criteria of 3 mm for 8 seconds).

NCT ID: NCT04122768 Completed - Clinical trials for Lung Transplantation

Activity Coaching in Patients Post Lung Transplantation

Start date: November 6, 2019
Phase: N/A
Study type: Interventional

Lung transplantation is an ultimate, effective treatment option for selected patients with end stage lung disease, improving quality of life and extending survival. Because of the improved survival during the last decades, enhancing the long term condition after lung transplantation has now become a focus for disease management. The co-presence of non-communicable diseases is common and poses new challenges to disease management. These comorbidities have been related to physical activity in the healthy population. As in other chronic respiratory disease, physical inactivity is a common feature of patients after LTX. Despite near normal lung function, exercise intolerance and physical inactivity persist up to years after the transplantation. Literature on effective interventions to increase physical activity are scarce in this population. Therefore, the present project aims to test the effectiveness of a tele coaching program to enhance physical activity and to analyze the association between physical activity and long-term health benefits in this population at risk. These research questions will be answered based on a randomized controlled trial. Patients that are active at baseline will be followed up in a cohort study.

NCT ID: NCT04121624 Completed - Technology Clinical Trials

Evaluation of a Novel Mobile Phone Application ( OptiBP) for Blood Pressure Monitoring

Start date: October 7, 2019
Phase:
Study type: Observational

Evaluation of a novel smartphone application designed to estimate blood pressure (systolic-diastolic and mean arterial pressure) and heart rate based on collected optical signals on patient's finger treated in the emergency department against the reference method (the oscillometric brachial cuff )

NCT ID: NCT04121104 Completed - Clinical trials for Failed Back Surgery Syndrome

Electrodermal Activity and Respiration in Patients Treated With Spinal Cord Stimulation

Start date: October 8, 2019
Phase: N/A
Study type: Interventional

This study is investigating skin conductance and respiration during on and off states of the spinal cord stimulator, in patients with failed back surgery syndrome.