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Anesthesia clinical trials

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NCT ID: NCT02793986 Completed - Anesthesia Clinical Trials

Dexmedetomidine vs Propofol Sedation Reduces Postoperative Delirium in Patients Receiving Hip Arthroplasty.

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

With blocks of lumbar and lumbar plexus, we can reduce the intravenous anesthetics usage. To offer an satisfied surgery process for patients, a proper sedation is necessary. So in this study, we want to investigate the influence of two different sedative drugs on outcomes of patients received hip replacement surgery .

NCT ID: NCT02787031 Completed - Anesthesia Clinical Trials

Variations in Anesthesia Care for Hip Fracture Surgery

Start date: April 2002
Phase: N/A
Study type: Observational

The investigators will use health administrative data to examine the variation of anesthesia type for hip fracture surgery, as well as sources of variation and predictors of variation.

NCT ID: NCT02786862 Completed - Anesthesia Clinical Trials

A Unique Device for Independent Lung Ventilation

Start date: March 2009
Phase: N/A
Study type: Interventional

Adequate blood oxygenation and ventilation/perfusion matching should be the main goal of anaesthetic and intensive care management. At present, the sole method of improving gas exchange restricted by ventilation/perfusion mismatching is independent ventilation with two ventilators. Recently, however, a unique device has been developed, enabling ventilation of independent lungs in 1:1, 2:1, 3:1, and 5:1 proportions. The main goal of the study was to evaluate the device's utility, precision and impact on biomechanical lung parameters during thoracic surgery under general anaesthesia with double lumen tube intubation. Secondly- to measure the gas distribution in supine and lateral decubitus position.

NCT ID: NCT02783443 Completed - Anesthesia Clinical Trials

Effect General and Regional Anesthesia on Glycocalyx

Start date: June 2016
Phase:
Study type: Observational

Observational study evaluating effect general or regional anaesthesia on glycocalyx by using perfused Boundary Region in sublingual microcirculation.

NCT ID: NCT02779998 Completed - Anesthesia Clinical Trials

Prophylactic Non-invasive Ventilation During Surgical Procedure in Rhythmology

VNI-RYTHMO
Start date: January 2017
Phase: N/A
Study type: Interventional

Acute respiratory failure is frequent during rhythmology procedure under light sedation in high risks selected patients. Non invasive ventilation (NIV) is recommended for acute cardiogenic pulmonary oedema and sleep apnea. The investigators will perform a monocentric, prospective, randomized controlled trial to compare the efficacy of NIV which associated pressure support ventilation (PSV: 5 to 15 cmH2O) and positive end expiratory pressure (PEEP: 5 to 10 cmH2O) with standard oxygen therapy in prevention of peroperative respiratory event. Our hypothesis is that peroperative use of NIV should reduce the incidence of apnea and hypoxia during procedure in rhythmology under light sedation.

NCT ID: NCT02778984 Completed - Anesthesia Clinical Trials

Facial Mask Tightness: A Comparative Study

EMAF
Start date: May 2016
Phase: N/A
Study type: Interventional

A correct preoxygenation can be obtained after a 3min delay of calm ventilation through a tight mask thereafter mask is used to make the patient breathing before intubation. Most tight masks are actually sold but they have never been compared in studies. The aim of this study is to compare air leaks with standard facial mask and QuadraLite masks during preoxygenation and induction of anesthesia.

NCT ID: NCT02766894 Completed - Anesthesia Clinical Trials

Adequate Depth of Anesthesia: the Anesthesiologist`s Assessment and the EEG Processed Monitoring

Start date: May 2016
Phase: N/A
Study type: Observational

Comparison of conventional assessment of anesthetic depth by anesthesiologists (moderate, deep or light anesthesia) with EEG monitoring (Narcotrend® state/index). In case of mismatch statistical analysis for underlying factors are done.

NCT ID: NCT02764502 Completed - Anesthesia Clinical Trials

Identification of Epidural Space Description of New Technique

Start date: March 2012
Phase: N/A
Study type: Interventional

Introduction Several attempts have been made to improve or facilitate epidural space detection beside conventional loss of resistant technique. Recently many sophisticated equipment's and techniques have been described which did not received widespread popularity. Objectives The Investigator describes and assesses the validity of using Pressure Gauge Manometer to confirm correct detection of lumber epidural space, in an inexpensive way. Methods Tuohy needle is introduced into intervertebral space at the level of L3-L4 up to the interspinous ligaments ( nearly 2cm mark on the needle).A3-way stopcock is connected to the hub of Tuohy needle with the in-line port of the stopcock attached to an air-filled 10 ml syringe. Using a 75 cm extension tube set and create a 30 mm Hg pressure gradient between manometer and the tip of epidural needle , the needle is advanced slowly using both hands while monitoring the manometer reading and is stopped when the pressure suddenly dropped ( the pressure usually drops by 5-10 mm Hg when the tip of the needle inters the epidural space ).

NCT ID: NCT02763098 Completed - Anesthesia Clinical Trials

Remifentanil on Hemodynamic Response to Anesthesia Induction

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

Effects of different doses of remifentanil on hemodynamic response to anesthesia induction in elderly patients ABSTRACT OBJECTÄ°VE: The investigators compared the effects of three different doses of remifentanil infusion, which have been performed for the induction of anesthesia in elder patients, on cardiovascular response. PATIENTS AND METHODS: The present study was designed as a randomized, prospective and double-blind study. A total of 90 ASA I-II patients over the age of 65 years were enrolled and each group consisted of 30 subjects. The patients were randomly (by lot) assigned to receive one of the three doses of remifentanil infusion (0.1, 0.2 or 0.3 µg/kg/min) for two minutes. Subsequently, 0.5 mg/kg propofol was administered via IV route and, 0.5 mg/kg rocuronium was administered via IV route at the time eyelash reflex disappeared. Intubation was performed after two minutes. After recording baseline values of heart rate (HR), systolic arterial pressure (SBP), diastolic arterial pressure (DBP) and mean arterial pressure (MAP), these values were recorded at the 1st, 2nd, 3rd, 4th and 5th minutes of induction.

NCT ID: NCT02757820 Completed - Anesthesia Clinical Trials

A Randomized Comparison of Pediatric I-gel, Air-Q With Classic Laryngeal Mask Airway

I-gelvsAir-q
Start date: June 14, 2016
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this randomized trial will be to evaluate the clinical performance of the I-gel, air- Q ILA compared with the LMA classic in pediatric patients undergoing peripheral surgery under general anesthesia.