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General Anesthesia clinical trials

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NCT ID: NCT01219322 Unknown status - General Anesthesia Clinical Trials

Intravenous Sodium Bicarbonate Verifies Intravenous Position of Catheters in Anesthetized Children

Start date: October 2010
Phase: Phase 1
Study type: Interventional

Extravasation is an unintentional injection or leakage of fluids in the perivascular or subcutaneous space. Extravasation can be associated with tissue injury with various level of severity and long term consequences. Currently the confirmation of intravenous location of the Intravenous (IV) catheter requires close observation of the insertion site with sufficient infiltration in the perivascular area to allow detection of swelling, discoloration and discomfort. Under Anesthesia direct observation is frequently prohibited. IV sodium bicarbonate (SB) is used frequently to treat different metabolic conditions and is known to cause a temporary elevation of exhaled carbon dioxide. This study aim is to evaluate the safety and efficacy of intravenous SB as a detector of intravenous placement of an IV line in anesthetized patients. Patients and Methods: The study has three parts, in part 1, the safety of subcutaneous injection of sodium bicarbonate was evaluated in 6 rats. In each animal the macroscopic and microscopic effects were evaluated and a safe dilution was determined. In the second part of the study the investigators will evaluated the efficacy of IV diluted SB to detect the proper location of IV catheters. 20 adult patients age 20 to 50 years will be enrolled. Patients all under general anesthesia with standard controlled ventilation via endotracheal tube. The correct placement of IV catheter will be confirmed by easy aspiration of blood from newly placed IV catheter. In each patient a bolus of 50 cc of 0.5 meq/cc SB or volume equivalent of normal saline will be injected in random order. The data collection will include patient's demographics, the presence or absence of an increase in the expired end-tidal carbon dioxide, onset and peak changes of end-tidal carbon dioxide as well as the hemodynamic changes after each injection.

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: NCT01179100 Withdrawn - Elderly Clinical Trials

How Lidocaine Affects Outcomes In Orthopedic Surgery Patients

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

This study will evaluate the effect of intraoperative lidocaine infusion on postoperative orientation and concentration in elderly patients having general anesthesia for orthopedic surgeries requiring a minimum 2 days hospitalization. This study will also aim to determine whether intraoperative lidocaine infusion during general anesthesia improves recovery and patient outcome, as well as to determine whether lidocaine infusion decreases postoperative opioid (pain medication) usage.

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.

NCT ID: NCT01041872 Completed - General Anesthesia Clinical Trials

Comparison of Different Propofol Formulations

Propofols
Start date: December 2009
Phase: Phase 4
Study type: Interventional

The objective of this study is to evaluate the influence of different propofol formulations(plain or with lidocaine)on anesthetic induction. Propofol plain or with lidocaine is administered using a closed-loop algorithm in order to reach a Bispectral Index target of 50.

NCT ID: NCT01035021 Completed - General Anesthesia Clinical Trials

Neuromuscular Block in Laryngeal Mask Airway(LMA) Insertion

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

The aim of this study is to evaluate the success rate, insertion time and complication depending on the use of neuromuscular blocking agent when inserting the laryngeal mask airway (LMA).