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Anaesthesia clinical trials

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NCT ID: NCT02805582 Completed - Anaesthesia Clinical Trials

Ultrasound Guided Intercostobrachial Nerve Block

Start date: August 2016
Phase: N/A
Study type: Interventional

The intercostobrachial nerve underlies many anatomical variations. For surgery of the upper arm the axilla is usually not anaesthetized by a brachial plexus block, which therefore needs to be completed by an intercostobrachial nerve block. The optimal access for an ultrasound guided block of the intercostobrachial nerve is not yet known. The investigators compare a proximal and a more distal approach to the nerve referred to onset time, sensory blocked area and duration.

NCT ID: NCT02801799 Terminated - Pain, Postoperative Clinical Trials

Effects of Local Anaesthetic Infusion Rates on Nerve Block Duration

Start date: October 10, 2016
Phase: Phase 1
Study type: Interventional

This trial is a part of the project: 'A novel technique for reliable, precise and safe postoperative pain management' (project no. 65-2014-3). The purpose of the trial is to investigate the effects of changing peri-neural infusion rates of ropivacaine 0.2% on the duration of nerve block. Intervention: Two intervention-days. Each day a peri-neural infusion of a fixed volume of ropivacaine 0.2% is to be infused in one of five infusion rates, using a peri-neural catheter. Intervention day 1: Focus on the common peroneal nerve. Intervention day 2: Focus on the sciatic nerve.

NCT ID: NCT02739399 Completed - Anaesthesia Clinical Trials

Effects of Phenylephrine on Cardiac Preload

Start date: February 2016
Phase: Phase 4
Study type: Interventional

In patients under general anesthesia, episodes of hypotension are often treated with phenylephrine. The effect of phenylephrine is conventionally attributed to afterload increase. The aim of the study is to describe the time course of the effects of phenylephrine on the cardiac preload and cardiac output, and to evaluate whether phenylephrine, as an exclusive alpha-mimetic, could be beneficial for preload optimisation.

NCT ID: NCT02664142 Completed - Anaesthesia Clinical Trials

BIS Monitoring of the Depth of Anaesthesia in Children

Start date: June 2015
Phase: N/A
Study type: Interventional

General anaesthesia (GA) is, according to many definitions, the greatest gift presented to the medical art (S. B. Nuland). One of the aims of GA is to achieve the optimal depth of anaesthesia and rapid emergence from general anaesthesia. In order to achieve this goal, it is necessary to observe the clinical condition of the patient, and at the same time monitor the patient's overall condition. With the currently available options of GA management (e.g. use of intravenous anaesthetics, strong analgesics and modern volatile anaesthetics, in combination with various methods of topical anaesthesia) the importance of methods measuring the depth of GA increases. The depth of GA may be defined as a continuous progressive decreasing of the central nervous system, together with a decreased reactivity to stimuli. In the course of GA, perioperative awareness is detected in 0.1-0.2% of cases. Awakening during a surgical procedure may result in significant psychological complications (e.g. post-traumatic stress disorder), and the patient may suffer from a serious long-time disorder.

NCT ID: NCT02662322 Completed - Anaesthesia Clinical Trials

Effect of Language and Confusion on Pain During Peripheral Intravenous Catheterization (KTHYPE)

KTHYPE
Start date: March 10, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to compare three communications during peripheral intravenous catheterization and measure pain patient: one hypnotic, confusion (HYPNOSIS), an other with negative connotation (NOCEBO) and at least with neutral connotation (NEUTRAL).

NCT ID: NCT02595788 Recruiting - Obesity Clinical Trials

Haemodynamic Changes During Anaesthesia in the Prone Position, Evaluated Using Transoesophageal Ultrasound

Start date: March 2014
Phase: N/A
Study type: Observational

Transoesophageal ultrasound examination before and after prone position.

NCT ID: NCT02481791 Recruiting - Heart Diseases Clinical Trials

Study to Evaluate the Optimal Dose of Remifentanil During MRI of the Heart Under General Anaesthesia

Start date: July 2015
Phase: Phase 3
Study type: Interventional

What is the optimal maintenance dose of remifentanil to ensure apnoea, during breath hold episodes in children having cardiac MR imaging with general anaesthesia?

NCT ID: NCT02442609 Completed - Anaesthesia Clinical Trials

Internet for Anesthesia Information : a Patient Questionaire

e-anesth
Start date: May 2015
Phase: N/A
Study type: Observational [Patient Registry]

Patients need information for perioperative period and internet may be an interesting alternative.This study analysed by questionaire what does patient look on internet: information of perioperative period and specifically for anesthesia. Questionaire (8 questions) are distributed to the patient before surgery and after they were prepared by surgeon. Population : adult (> 18 y), no emergency procedure.The mean question is the use of internet for anesthesia information.

NCT ID: NCT02350348 Completed - Children Clinical Trials

NEonate-Children sTudy of Anaesthesia pRactice IN Europe Epidemiology of Morbidity and Mortality in Neonatal Anaesthesia

NECTARINE
Start date: March 2016
Phase:
Study type: Observational

To study the 30-day morbidity and mortality after neonatal anaesthesia, and predictive factors that can be responsible for poor outcome.

NCT ID: NCT02314078 Completed - Pregnancy Clinical Trials

Audit of the Response Time of the Anaesthetic and Surgical Techniques for Crash Caesarean Section

Crash
Start date: January 2010
Phase: N/A
Study type: Observational

A decision-to-delivery interval of 30 minutes for category-1 Caesarean section deliveries is the standard of practice recommended by clinical guidelines.