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Anesthesia clinical trials

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NCT ID: NCT01579864 Terminated - Anesthesia Clinical Trials

Succinylcholine or Rocuronium for Rigid Bronchoscopy Under General Anesthesia

Broncho-SR
Start date: January 2012
Phase: Phase 4
Study type: Interventional

Myorelaxation is generally used as a part of general anesthesia for interventional rigid bronchoscopy. Succinylcholine is most often used because its short duration of action but rocuronium can be used since sugammadex permits a rapid and complete reversal of the neuromuscular block. The aim of ths study is to compare both agents.

NCT ID: NCT01474824 Terminated - Anesthesia Clinical Trials

Validation of Nexfin Cardiac Output in Elderly Patients With Hip Fracture

Start date: January 2013
Phase: N/A
Study type: Observational

Measurement of how much blood the heart pumps may be useful in guiding how much intravenous fluid to give patients during surgery. The current monitors either require special drips (arterial and/or central lines) or a probe inserted into the oesophagus (food pipe) which may limit their use. Newer monitors are available which are completely non-invasive and seem to work well in younger patients. Patients with hip fracture are elderly and frail. The investigators wish to see whether the newer non-invasive monitor works well enough compared to the current monitors in this group of patients. If it does this may allow more of these patients to be monitored in this way.

NCT ID: NCT01136668 Terminated - Anesthesia Clinical Trials

Transversus Abdominis Plane Block in Children Undergoing Ostomy Surgery

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

The primary objective of this study is to determine if the use of Transversus Abdominis Plane (TAP) blocks reduce early postoperative opioid requirements.

NCT ID: NCT01017237 Terminated - Anesthesia Clinical Trials

Dexmedetomidine Sedation With Third Molar Surgery

Start date: July 2009
Phase: Phase 4
Study type: Interventional

Intravenous sedation is used frequently for the relief of pain and anxiety associated with oral surgical procedures performed under local anesthesia. The purpose of this study is to learn about patient and surgeon satisfaction with sedation using Dexmedetomidine in combination with midazolam alone or with midazolam plus low dose ketamine while having wisdom teeth removed. The sedation produced by dexmedetomidine is unique in that it mimics natural sleep, a unique quality not shared by other drugs. Dexmedetomidine is often used in anesthesia in hospital operating rooms and has been approved by the US Food and Drug Administration for the use planned in this study.

NCT ID: NCT00969189 Terminated - Anesthesia Clinical Trials

Evaluation of the Pediatric Igel Airway in 250 Children

Start date: August 2009
Phase: N/A
Study type: Observational

Once a child has been anaesthetised and is fully asleep, a special airway tube called a laryngeal mask is often inserted into their mouth to help with their breathing. This tube is removed just before the child wakes up. A new type of airway tube, called an i-gel airway, has been developed for children, which is hoped will be easier to insert, safer once in position, and will be less likely to cause a sore throat after the anaesthetic than a standard laryngeal mask. The adult i-gel airway has been available for adults since 2007, and early trials have shown very encouraging results.

NCT ID: NCT00922467 Terminated - Anesthesia Clinical Trials

Influence of Esmolol on a Closed-Loop Anesthesia System

Start date: June 2009
Phase: Phase 3
Study type: Interventional

Main objective is to evaluate the sparing effect of esmolol on the required doses of propofol and remifentanil

NCT ID: NCT00910416 Terminated - Anesthesia Clinical Trials

The Comparability of Bispectral Index and Neurosense During Anesthesia

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

The assessment of anesthesia depth was based, until recently, on the evolution of hemodynamic parameters. Nowadays it can be evaluated by several monitoring methods, derived from electroencephalogram analysis, namely the Bispectral Index (Aspect Medical Systems, Newton, USA). A new modality is currently under development: the NeuroSENSE (Cleveland Medical Devices Inc., Cleveland, OH 44103, USA). The goal of this study is to compare both monitoring modalities during anesthesia.

NCT ID: NCT00894751 Terminated - Anesthesia Clinical Trials

Two Anesthetic Techniques in Magnetic Resonance Imaging (MRI)

Start date: January 2009
Phase: Phase 1
Study type: Interventional

The goal of this study is to determine if there is a significant difference in the quality of care between the investigators' two standard anesthesia techniques for children undergoing a MRI of the body and/or extremity MRI. Quality of care will be measured by time spent in the MRI room as well as parental satisfaction, frequency of interruptions of the MRI scan, incidence-severity of respiratory complications, post anesthesia agitation, and time spent in the induction room, MRI room, and Post-Anesthesia Care Unit (PACU).

NCT ID: NCT00779844 Terminated - Obesity Clinical Trials

Anesthesic Propofol and Remifentanil Requirements in Obese Patients

LoopObese
Start date: December 2008
Phase: Phase 4
Study type: Interventional

Pharmacokinetic models for anesthetic agents are questionable. The objective of the study is to compare the propofol and remifentanil doses required to maintain the bispectral index in the range 40-60 in two groups of patients: obese patients and lean patients

NCT ID: NCT00778505 Terminated - Anesthesia Clinical Trials

Use of Closed-loop Anesthesia in Pediatric Patients

LoopPed
Start date: October 2008
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 pediatric anesthesia