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General Anesthesia clinical trials

View clinical trials related to General Anesthesia.

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NCT ID: NCT00741507 Completed - General Anesthesia Clinical Trials

Unhealthy Alcohol Drinking and Anesthetic Requirement in Women

UNADAREW
Start date: September 2008
Phase: N/A
Study type: Interventional

Unhealthy alcohol drinking is negatively influencing health of people and costing a large number of annual finance via "secondhand" effects. Additionally, unhealthy alcohol use covers a spectrum that is associated with varying degrees of risk to health. The investigators hypothesized that unhealthy alcohol drinking resulted in significant increase in anesthetic requirement during general anesthesia. This investigation would clarify the association between unhealthy alcohol use and the intraoperative consumption of anesthetics, and provide clinical evidence for preoperative assessment with respect to the alcohol drinking habit.

NCT ID: NCT00670826 Not yet recruiting - General Anesthesia Clinical Trials

Comparison Study of Intraoperative Patient Warming Systems

Start date: July 2008
Phase: N/A
Study type: Interventional

Medications used to put people to sleep during surgical procedures also cause changes in the body's ability to control its temperature. These changes can make a person's temperature drop below normal. To minimize this drop in body temperature, different types of body warming products are used during surgery. This study is designed to compare the the temperatures of people under general anesthesia after 60 minutes of warming with each product. The study hypothesis is that the people warmed with the Dynatherm Medical vitalHEAT vH2 System will decrease less in the first 60 minutes of warming time than people warmed with the Arizant Bair Hugger System.

NCT ID: NCT00627081 Completed - General Anesthesia Clinical Trials

Effect of Thoracic Epidural Analgesia on Intravenous Closed-Loop Anesthesia

Drone-APDT
Start date: February 2008
Phase: Phase 4
Study type: Interventional

The association of general anesthesia and of thoracic epidural anesthesia is used in thoracic surgery with a demonstrated benefit on the risk of postoperative respiratory complications. The objective of the study is to analyze the influence of thoracic epidural administration of chirocaine (5 mg/ml) on the administration of anesthetic agents (propofol and remifentanil), these drugs being administrated using a closed-loop system with the Bispectral Index as the controller. Two groups of patients are compared: - one group will receive general anesthesia and thoracic epidural administration of saline. Chirocaine will be administered before patient's awakening, - one group will receive general anesthesia and thoracic epidural administration of chirocaine (5 mg/ml). In both groups, the closed-loop system ensures that le depth of anesthesia is similar in both groups.

NCT ID: NCT00614588 Completed - Surgery Clinical Trials

Temperature Measurement in Post-Anesthesia Care Units

Start date: January 2008
Phase: N/A
Study type: Observational

This study will evaluate the accuracy of several thermometers and temperature changes during surgery and immediately after surgery.

NCT ID: NCT00599066 Completed - General Anesthesia Clinical Trials

Intraoperative M-Entropy Measurements

Start date: September 2007
Phase: N/A
Study type: Observational

The purpose of this study is to learn more about an Entropy monitor that the anesthesiologist will be using.

NCT ID: NCT00532402 Completed - General Anesthesia Clinical Trials

Continuous and Discontinuous Determination of Propofol Concentration in Breathing Gas

Start date: September 2007
Phase: N/A
Study type: Observational

This study should compare the propofol concentration in breathing gas and in plasma (before and) after lung passage. Propofol concentrations in breathing gas are continuously measured by a sensor. For comparison a discontinuous method is used. Neurophysiologic parameters for determination of depth of anesthesia are compared to the continuous measured propofol concentration in breathing gas. Study hypothesis: continuous measured propofol concentration in breathing gas correlates to propofol concentration in plasma and depth of anaesthesia.

NCT ID: NCT00492453 Recruiting - Postoperative Pain Clinical Trials

Spinal Versus General Anesthesia for Laparoscopic Cholecystectomy

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

The purpose of the study is to assess whether spinal anesthesia is or not superior to the standard general anesthesia for fit patients undergoing laparoscopic cholecystectomy.

NCT ID: NCT00468494 Completed - Hyperglycemia Clinical Trials

Can Blood Glucose Levels During the Perioperative Period Identify a Population at Risk for Hyperglycemia?

Start date: September 2006
Phase: N/A
Study type: Observational

Surgery performed during general anesthesia induces a stress effect on the body. Our plan is to identify population at risk of hyperglycemia during perioperative period.

NCT ID: NCT00434382 Active, not recruiting - General Anesthesia Clinical Trials

Neuronal Mechanisms of Sensory Processing During General Anesthesia

BEO
Start date: October 2002
Phase: N/A
Study type: Interventional

The ability of Mid Latency Auditory Evoked Potentials for a routine monitoring of sensory suppression should be evaluated during a wide spectrum of clinically common forms general anesthesia.