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General Anesthesia clinical trials

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NCT ID: NCT01342510 Completed - General Anesthesia Clinical Trials

Combination of Magnesium and Lidocaine for the Pretreatment of Pain That is Caused by the Injection of Propofol

Start date: April 2011
Phase: Phase 4
Study type: Interventional

Since the introduction of propofol into routine anesthesia practice, the phenomena of pain on injection has plagued anesthesia providers. Propofol, an unstable phenol, triggers the release of bradykinin on injection. This release causes a painful burning sensation in the patient at the site of injection. Anesthesia providers have attempted a large number of remedies to prevent this pain on injection. Previously explored ideas include injecting propofol into larger veins, warming of the hand with hot packs, and intravenous pretreatment with numerous other medications. Currently, pretreatment with lidocaine is commonly administered to prevent propofol injection pain. No studies to date have looked at the combination of lidocaine and magnesium in a single syringe for the pretreatment of pain on injection caused by propofol. In addition, the administration protocols that have been studied thus far do not mirror clinical practice at the University of Wisconsin. The investigators propose studying the use of magnesium and lidocaine in a single syringe for pretreatment of propofol related pain on injection.

NCT ID: NCT01269099 Completed - General Anesthesia Clinical Trials

Hypokalemia and Intravenous Patient Controlled Analgesia

Start date: January 2010
Phase: N/A
Study type: Interventional

The increase in stress hormone level and hyperventilation caused by the postoperative pain may contribute to the development of hypokalemia during postoperative period. Therefore, if the postoperative pain is well controlled by the IV-PCA,the plasma potassium level during the postoperative period may be not affected by stress response. The researchers tried to investigate the effect of IV-PCA on potassium regulation during the postoperative period.

NCT ID: NCT01267916 Completed - General Anesthesia Clinical Trials

Intrinsic PEEP During Mechanical Ventilation of Patients With Obesity

Start date: January 2011
Phase: N/A
Study type: Interventional

It is demonstrated that expiratory flow limitation and as a consequence, intrinsic positive end-expiratory pressure (PEEP) is present in grossly obese subjects especially in the supine position. The investigators tried to investigate the effect of low respiratory rate and high tidal volume on the intrinsic PEEP and gas exchange for obese subjects undergoing general anesthesia.

NCT ID: NCT01265862 Completed - General Anesthesia Clinical Trials

Does the Use of the GlideRite® Endotracheal Tube in Combination With the I-gel® Improve Intubation Success Rate?

Start date: April 2011
Phase: N/A
Study type: Interventional

The investigators aim to compare two different types of supraglottic devices for tracheal intubation in patients undergoing elective surgery under general anesthesia. The investigators hypothesis is that the use of the I-gel® supraglottic airway device associated with a GlideRite® endotracheal tube will result in an equal success rate of fiberoptic tracheal intubation when compared to the LMA-Fastrach® associated with a GlideRite® endotracheal tube. Time to intubate with the I-gel® device should also be shorter.

NCT ID: NCT01212536 Completed - Children Clinical Trials

Airtraq Versus Conventional Laryngoscopy in Children

Start date: August 2010
Phase: N/A
Study type: Interventional

The investigators aim to compare the new paediatric Airtraq indirect optical laryngoscope with conventional direct laryngoscopy for tracheal intubation in a randomised crossover study during routine anaesthesia. The investigators hypothesise that the Airtraq is as good as conventional laryngoscopy for tracheal intubation of infants and children. This will be an equivalence rather than a non-inferiority study.

NCT ID: NCT01198639 Completed - General Anesthesia Clinical Trials

One-year Mortality After Surgery and Low Bispectral Index

ELA
Start date: September 13, 2010
Phase: N/A
Study type: Interventional

A correlation between deep anesthesia (defined as time with Bispectral Index (BIS) lower than 45) and death within 1 yr after surgery has previously been reported. In order to confirm or refute these findings, the investigators have designed a study which compares two methods of administration for total intravenous anesthesia (propofol and remifentanil): - manual administration: the anesthesiologists are instructed to maintain the BIS value between 40 and 60. - closed loop administration: an algorithm is used to maintain the BIS value between 40 and 60. Based on previous studies, the amount of time that BIS is maintained above 40 is greater when anesthetics agents are administered using closed loop compared with manual administration.

NCT ID: NCT01191021 Completed - General Anesthesia Clinical Trials

Monitoring Exhaled Propofol to Individualize General Anesthesia

EPIGA
Start date: August 2010
Phase: Phase 1
Study type: Interventional

This trial investigates the relationship between concentrations of the anesthetic drug propofol in exhaled breath, blood and drug effect in volunteers undergoing general anesthesia. The main goal of this study is to develop a pharmacokinetic - and dynamic model for propofol in exhaled breath.

NCT ID: NCT01154660 Completed - Surgery Clinical Trials

Effects of Increased Tidal Volume on Internal Jugular Vein Cross-sectional Area

Start date: July 2010
Phase: N/A
Study type: Interventional

As increasing tidal volume, the cross sectional area and circumference of Internal Jugular Vein (IJV) could increase. And In the previous study, Trendelenburg position can increase size of IJV. So investigators would compare the cross sectional area, circumference of IJV and peak airway pressure in neutral and Trendelenburg position

NCT ID: NCT01096212 Completed - General Anesthesia Clinical Trials

Efficacy and Safety of Sevofran in Patients Scheduled for Elective Surgery Under General Anesthesia

Start date: September 2008
Phase: Phase 4
Study type: Interventional

Sevoflurane is currently being used in more than 100 countries worldwide with an estimated 100 million operations having been performed using sevoflurane as a general anesthetic. After the expiry of the patent on sevoflurane as a pharmaceutical drug, a generic product (Sevofran®; Hana pharmacy, Co. Ltd, Seoul, Korea) has been launched. The aims of this study were to investigate the efficacy (mean minimum alveolar concentration), recovery characteristics (time to recovery of consciousness (ROC) and recovery, and BIS values at ROC and orientation), and safety (incidence and severity of adverse events) of generic sevoflurane in patients undergoing elective surgery.

NCT ID: NCT01091350 Completed - General Anesthesia Clinical Trials

Influence of Equilibration Rate Constant (ke0) of Propofol on the Effect Site Concentration for Loss of Consciousness

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

The aim of this study is to validate that an effect compartment concentration for loss of consciousness (LOC) was varied according to different Keo value.