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Respiratory Insufficiency clinical trials

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NCT ID: NCT02845128 Completed - Validation Clinical Trials

Prospective Validation of the ROX Index

Start date: May 2016
Phase:
Study type: Observational

We recently described the ROX index, defined as the ratio of SpO2/FIO2 to respiratory rate that outperformed the diagnostic accuracy of the two variables separately. Patients who had a ROX index ≥4.88 after 12 hours of HFNC therapy were less likely to be intubated, even after adjusting for potential covariates. Like any other scoring system, an independent validation of the score in a different population is necessary. We therefore undertook a multicenter, prospective study to validate the ROX index's diagnostic accuracy for determining which patients will fail on HFNC and will need to be intubated.

NCT ID: NCT02845076 Completed - Weaning Failure Clinical Trials

Weaning From Noninvasive Ventilation

WEANIV
Start date: September 2016
Phase: N/A
Study type: Interventional

Noninvasive ventilation (NIV) weaning strategies differ considerably from one another. These strategies have yet not been compared to each other. Therefore, the investigators planned to perform a prospective, randomized, pilot study involving hypercapnic acute respiratory failure patients ready to be weaned off from NIV. The investigators are going to compare the success rate of NIV weaning and the duration of NIV after randomization between 3 NIV weaning methods: gradual decrease in duration of NIV or level of ventilator support, and abrupt discontinuation of NIV.

NCT ID: NCT02841592 Completed - Clinical trials for Acute Respiratory Failure

Non-rebreather at Flush Rate Compared to Bag Valve Mask With Assist

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

This crossover investigation enrolls healthy volunteers and compares the exhaled oxygen content (FeO2) between the non-rebreather mask at the flush rate and a bag-valve-mask device at the flush rate, used with active positive pressure assistance.

NCT ID: NCT02837055 Completed - Clinical trials for Respiratory Insufficiency

Conventional Intubation Versus VivaSight™-SL

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

It has been shown that videolaryngoscopy may be superior to direct laryngoscopy for endotracheal intubation in intensive care. Recently, an endotracheal tube with an integrated camera at its tip has been introduced (VivaSight-SL) allowing for direct visual confirmation of the tube's passage through the vocal cords during intubation. Patients who are requiring urgent or endotracheal intubation in intensive care are randomized to receive either a conventional intubation with direct laryngoscopy or to receive intubation with the VivaSight-SL-Tube. Primary outcome measures are first attempt success rate and number of attempts to successful intubation.

NCT ID: NCT02834325 Completed - Pneumonia Clinical Trials

Predicting Success of HFNC: The Utility of the ROX Index

Start date: January 2009
Phase: N/A
Study type: Observational

The purpose of the study was to describe early predictors and to develop a prediction tool that accurately identifies the need for mechanical ventilation in pneumonia patients with acute respiratory failure treated with High Flow nasal cannula.

NCT ID: NCT02825615 Completed - Clinical trials for Acute Respiratory Failure

Better Arterial Cannulation Technique With Different Hemodynamics

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

Purpose Two techniques of radial artery cannulation, ultrasound guided (USG) and conventional method (CM) were compared to find the better technique in general and in different hemodynamic subsets of patients. Method This is a prospective randomized, single center study of 100 patients. The details of the primary cannulation technique, number of attempts, time taken, failure and cross-over technique were recorded for three different hemodynamic subsets with Systolic blood pressure <80 mm hg, 80-100 mm hg and > 100 mm hg.

NCT ID: NCT02822170 Completed - Clinical trials for Acute Respiratory Failure

A Pilot Study of Combined Cycle Ergometry and Amino Acids in the ICU

Start date: June 2016
Phase: N/A
Study type: Interventional

The purpose of this small pilot study is to refine a combined intervention of IV amino acids and cycle ergometry in critically ill patients, and to gather preliminary data, before proceeding with a larger multi-center RCT. A total of 10 patients will receive the combined intervention.

NCT ID: NCT02822001 Recruiting - Clinical trials for Respiratory Insufficiency

Sugammadex vs. Placebo to Prevent Residual Neuromuscular Block in the Post--‐Anesthesia Care Unit

Sugammadex
Start date: February 16, 2017
Phase: Phase 4
Study type: Interventional

The Primary objective of this study is to determine whether patients who receive sugammadex immediately after tracheal extubation will exhibit a decrease in the incidence of postoperative residual paralysis and an associated decrease in the incidence of postoperative respiratory depression (which can precede critical respiratory events, CRE). The Secondary objectives are to: a) determine whether patients receiving sugammadex will have a normal TOF ratio (>0.90) indicative of full neuromuscular recovery in the PACU; and b) to improve patient safety by documenting whether postoperative respiratory depression (decreased MV below 80% and 40% of predicted MV as assessed by a Respiratory Volume Monitor) is due to opioid administration vs. postoperative residual neuromuscular block (by comparing postoperative VAS scores and total opioid administered).

NCT ID: NCT02821429 Withdrawn - Clinical trials for Respiratory Insufficiency

Respiratory Weaning Following Cardiac Surgery.

ETCCCV
Start date: January 2015
Phase:
Study type: Observational

Respiratory weaning failure worsens prognostic of patients following on-pump cardiac surgery. There are increasing evidences that pulmonary, diaphragmatic or cardiologic echographies are useful in order to improve this critical medical status. Based both on a previous study conducted in the critical care unit of Purpan and on literature we hypothesize that a combined thoracic echography score could be of interest. We make the hypothesis that the use of a score based on thoracic combined echography (ETC = cardiac, pulmonary and diaphragmatic) allows to predict the failure of respiratory weaning in cardiac surgery and allows to improve the characterization of the causes of this failure

NCT ID: NCT02819661 Recruiting - Clinical trials for Respiratory Depression

Respiratory Depression in Women With BMI≥30 Underwent Spinal Anesthesia With Intrathecal Morphine in Elective C-section

Start date: May 1, 2018
Phase: N/A
Study type: Interventional

The study will examine whether there is a difference in the frequencies of respiratory depression among obese women receiving spinal anesthesia combined with opioids compared to women with normal BMI. If such a risk exists further investigation will be required to establish the proper criteria for the administration of morphine with spinal anesthesia to obese women.