Clinical Trials Logo

Anesthesia, General clinical trials

View clinical trials related to Anesthesia, General.

Filter by:

NCT ID: NCT00451217 Completed - Anesthesia, General Clinical Trials

Comparison of Sugammadex (Org 25969) With Neostigmine as Reversal Agents for Rocuronium or Vecuronium at Reappearance of T2 (P05960)

Start date: November 17, 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study was to demonstrate in adult participants faster recovery from a neuromuscular block induced by either rocuronium or vecuronium after reversal at reappearance of T2 (the amplitude of the first response of second twitch to train of four (TOF) stimulation, expressed as percentage of control first twitch, T1) by 2.0 mg/kg sugammadex (Org 25969) compared to 50 ug/kg neostigmine.

NCT ID: NCT00451100 Completed - Anesthesia, General Clinical Trials

Comparison of Rocuronium and Org 25969 With Cisatracurium and Neostigmine (19.4.310)(P05931)

Start date: November 10, 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study was to demonstrate in adult patients a faster recovery from a neuromuscular block with 2.0 mg/kg Org 25969 (sugammadex) after rocuronium as compared to 50 ug/kg neostigmine after cisatracurium when administered at reappearance of T2

NCT ID: NCT00392158 Completed - Anesthesia, General Clinical Trials

Manual Administration of Propofol-remifentanil Versus Dual Closed-loop Using Bispectral Index as the Control Variable

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

To compare manual administration of propofol and remifentanil and dual closed-loop using bispectral index as the control variable during anesthesia

NCT ID: NCT00391963 Completed - Anesthesia, General Clinical Trials

Comparison of the Bispectral Index and the Entropy of the Electroencephalogram During Total Intravenous Anesthesia

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

To compare Bispectral index and entropy during maintenance of anesthesia

NCT ID: NCT00391885 Completed - Anesthesia, General Clinical Trials

Target-controlled Infusion of Propofol and Remifentanil During General Anaesthesia Guided by Entropy

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

This study compares the manual administration of propofol and remifentanil and their delivery using a combined closed-loop anesthesia system, entropy of the EEG being the controller.

NCT ID: NCT00379613 Completed - Anesthesia, General Clinical Trials

Use of Sugammadex Administered at 5 Minutes After Administration of 1.2 mg/kg Esmeron® (19.4.205)(P05942)

Start date: November 7, 2003
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the optimal dose of sugammadex when this compound is administered during deep neuromuscular block. Sugammadex is administered shortly (5 minutes) after administration of a high dose (1.2 mg/kg) of the neuromuscular blocking agent rocuronium . Under these circumstance the neuromuscular block is deep. The safety and pharmacokinetics of sugammadex are also studied.

NCT ID: NCT00298831 Completed - Anesthesia, General Clinical Trials

Use of Sugammadex at the End of Case in Routine Anesthesia (MK-8616-023)

Start date: October 27, 2005
Phase: Phase 3
Study type: Interventional

The primary purpose of the study is to determine the time-course of recovery to a T4/T1 ratio of 0.9 within 4 minutes after 4.0 mg.kg^-1 Sugammadex is administered at least 15 minutes after the last administration of rocuronium in a wide range of surgical procedures and anesthetic regimens (routine use). Safety evaluation is part of the study.

NCT ID: NCT00165971 Completed - Anesthesia, General Clinical Trials

Recovery From General Anesthesia

Start date: December 2003
Phase: N/A
Study type: Interventional

General anesthesia allows people to have surgery without experiencing the procedure or pain. To remain unconscious, the depth of sleep must be monitored. Various monitors have been developed, one of which is BIS (short for bispectral index). BIS monitors the level of sleep during anesthesia and improves patient recovery because the amount of sleep drugs can be fine-tuned to the individual. Patients who need a lot to stay asleep get more, and those who need less get less. As a result, patients tend to wake up faster with BIS monitoring as compared to standard practice not using BIS. Little is known about the long-term effects of BIS monitoring. This study investigates whether BIS monitoring during anesthesia improves long-term outcome, well after surgery is over. The hypothesis is that it does. Two groups of patients are compared: one in which BIS monitoring was used, and one in which it was not. Groups are compared on tests of memory, concentration and mental well-being, to see if one does and feels better than the other. The investigators also take blood samples to see how well patients' bodies deal with the surgery. The investigators expect the BIS monitoring group to do better.