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Anesthesia clinical trials

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NCT ID: NCT00547209 Completed - Anesthesia Clinical Trials

Effect of Nitrous Oxide on Intravenous Closed-loop Anesthesia

Drone-N2O
Start date: October 2007
Phase: Phase 4
Study type: Interventional

The main objective of the study is to analyze the influence of nitrous oxide on propofol and remifentanil requirements.

NCT ID: NCT00522587 Completed - Anesthesia Clinical Trials

Sevoflurane-Remifentanil Interaction: Multiple Response Surfaces, Validation of Calibration Stimuli, Validation of the Intraoperative Isobole Concept and Investigating Remifentanil Induced Opioid Tolerance

Start date: April 2008
Phase: Phase 2
Study type: Interventional

During this study, the pharmacodynamic interactions between sevoflurane and remifentanil will be studied.

NCT ID: NCT00498251 Completed - Anesthesia Clinical Trials

Prevention of Lung Edema After Thoracic Surgery

Start date: September 2004
Phase: N/A
Study type: Interventional

Background : Acute lung injury (ALI) occasionally occurs after pulmonary resection and carries a bad prognosis with a high mortality rate ranging from 20 to 100%. Objectives : 1. to evaluate pre-, intra- and postoperative changes in hemodynamics, oxygenation indices as well as intra- and extravascular lung water using simple thermodilution technique and continuous arterial pressure analysis 2. to test the efficacy of inhaled beta2 -adrenergic agonist versus anticholinergic agents to reduce lung edema in patients undergoing thoracic surgery and in pigs subjected to lipolysacharide-induced ALI. Design of the research protocol: - Prospective controlled trial including surgical patients with high risk factors for ALI (n=60) allocated to receive inhaled drugs (randomised, double-blind, cross-over mode). - Main measurements: Intra-thoracic blood volume, intra- and extra-vascular lung water, hemodynamic parameters (CO, systolic arterial pressure/flow variations, dPmax, MAP, CVP), oxygenation indices (PaO2/FIO2), ventilatory parameters, clinical outcome data, histochemical and pathological data. Glossary CO = cardiac output; dPmax = maximal arterial pressure slope; SAP-V = systolic arterial pressure variations; Flow–V = Flow variations; MAP = mean arterial pressure; CVP = central venous pressure; PaO2=arterial oxygen pressure; FIO2= oxygen inspiratory fraction

NCT ID: NCT00481234 Completed - Anesthesia Clinical Trials

Heart Rate Variability for Prediction of Perioperative Events

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

Patients with underlying cardiovascular disease are at high risk of perioperative cardiovascular events and death. Hemodynamic variables are controlled by the autonomic nervous system reflected by Heart Rate Variability. To investigate whether differences of HRV parameters predict perioperative cardiovascular events.

NCT ID: NCT00421148 Completed - Anesthesia Clinical Trials

Dose-Finding Pediatric and Adult Trial With Sugammadex (Org 25969, MK-8616, SCH 900616) (19.4.306) (MK-8616-034) (P05961)

Start date: May 30, 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is: - to explore the dose-response relation of sugammadex (Org 25969, MK-8616, SCH 900616) given as a reversal agent at reappearance of T2 after 0.6 mg.kg-1 rocuronium in pediatric and adult participants - to explore the pharmacokinetics (PK) of sugammadex in pediatric and adult participants, and to evaluate the safety of sugammadex in pediatric and adult participants.

NCT ID: NCT00420680 Completed - Anesthesia Clinical Trials

Safety and Efficacy Evaluation of Sugammadex in Cardiac Patients (19.4.309)(P05934)

Start date: November 7, 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety of 2.0 mg/kg and 4.0 mg/kg sugammadex given as a reversal agent at reappearance of T2 after 0.6 mg/kg rocuronium in cardiac patients

NCT ID: NCT00398827 Completed - Anesthesia Clinical Trials

A Safety and Efficacy Study of Dexmedetomidine in Patients Requiring Sedation During Monitored Anesthesia Care (MAC)

Start date: December 2006
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the safety and efficacy of dexmedetomidine as compared to placebo when used for the sedation of subjects requiring monitored anesthesia care (MAC).

NCT ID: NCT00364637 Recruiting - Anesthesia Clinical Trials

Volatile Anesthetics in Cardiac Protection

Start date: January 2005
Phase: Phase 4
Study type: Interventional

Patients undergoing stenting procedures, or cardiac or non-cardiac surgery could develop myocardial damage as testified by cardiac troponin release. Sevoflurane (volatile anesthetic), routinely used in cardiac and non-cardiac anesthesia, has cardioprotective properties that could be useful to reduce cardiac damage, as indicated by cardiac troponin release in different contexts: - stenting procedures (periprocedural administration) - non-cardiac surgery (during the whole procedure) - cardiac surgery (during the whole procedure)

NCT ID: NCT00321191 Completed - Anesthesia Clinical Trials

Measurement of the Second Gas Effect on Sevoflurane in Anaesthetised Patients

Start date: May 2006
Phase: Phase 4
Study type: Interventional

This study is investigating the "second gas effect", a phenomenon produced by the uptake of nitrous oxide (N2O) by the lungs, during the course of a typical anaesthetic. The effect is to increase the concentration of other breathed gases in the lung. These include oxygen and volatile anaesthetic agents such as sevoflurane, which are also normally administered along with N2O. We wish to i) measure the magnitude of the second gas effects on both blood and expired concentrations of sevoflurane (Part 1), and ii) see if a demonstrable difference exists between the effects on blood and expired concentrations.

NCT ID: NCT00308984 Completed - Anesthesia Clinical Trials

CARE--Childhood Awareness and Recall Evaluation

Start date: January 2006
Phase: Phase 4
Study type: Observational

The purpose of this study is to describe the incidence of recall or awareness under anesthesia in children aged 5-15 by collecting anesthetic and post-operative follow-up data relating to intra-operative recall during general anesthesia. The hypothesis is that the implementation of routine awareness follow-up evaluation in children undergoing general anesthesia will identify that the incidence of intra-operative awareness in children is equal to or greater than in adults.