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Anesthesia, General clinical trials

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NCT ID: NCT03267979 Completed - Anesthesia, General Clinical Trials

Assessing Pain in the Postoperative Period by Automatically Measuring the Variation Coefficient of Pupillary Diameter: PREVANS Study

PREVANS
Start date: November 2, 2014
Phase: N/A
Study type: Interventional

Different pain assessment methods have been proposed to evaluate analgesic efficacy after surgical operation. Pain is a subjective phenomenon. Patient did his pain self assessment. But, cooperation of the patient is limited by cultural differences, language barriers or residual effect of products used while general anesthesia. A lot of study were conducted to demonstrate and to quantify the pain after an operation. The aim will be dose analgesic treatment better without cooperation of the patient. This sudy concerns patients on the post anesthesia care units one hour after their arrival. They will have electrocardiogram and video-pupillometer.

NCT ID: NCT03239678 Completed - Anesthesia, General Clinical Trials

Safe Time for Apnea After Preoxygenation

STAP
Start date: August 1, 2017
Phase: N/A
Study type: Interventional

The use of 100% oxygen during the induction of general anesthesia is always preferable to have enough time to secure the airway by endotracheal intubation, because preoxygenation with a low oxygen concentration may reduce the safe time for apnea. However, using a low oxygen concentration during preoxygenation might prevent the formation of atelectasis. There is still no clear conclusion about the best oxygen concentration for preoxygenation. Our study is designed to evaluate the safety of preoxygenation with 80%, 60%, 40%, 30% and 21% oxygen by the safe time for apnea during the induction of general anesthesia.

NCT ID: NCT03155555 Completed - Clinical trials for Mechanical Ventilation

Comparison of Carotid Peak Systolic Velocity Variation With Aortic Peak Systolic Velocity Variation in Pediatric Non-Cardiac Surgery

Start date: December 2016
Phase:
Study type: Observational

The purpose of this study is to evaluate whether carotid Doppler peak systolic velocity can be an easy to measure possible surrogate for echocardiographic measurement of aortic peak systolic velocity variation which is an index of fluid responsiveness in mechanically ventilated children intra-operatively.

NCT ID: NCT03083457 Completed - Surgery Clinical Trials

Physiological Effects of Lung Recruitment During General Anesthesia and Low-tidal Volume Ventilation

PEEP-RM
Start date: March 20, 2017
Phase: N/A
Study type: Interventional

Low-tidal volume ventilation is arising as a tool to optimize the ventilatory management and to improve clinical outcome in patients undergoing general anesthesia for abdominal surgery. A recent large randomized controlled trial failed to detect a significant difference between two different approaches for ensuring adequate lung recruitment (PEEP=12 cmH2O + scheduled recruiting maneuvers vs. PEEP 2 cmH2O) during protective ventilation. Thus, in patients undergoing open abdominal surgery and receiving low-tidal volumes, the effects of different positive end-expiratory pressure (PEEP) levels and recruiting maneuvers remain to be established. Design: prospective, cross-over, physiological trial. PURPOSE To assess the physiological effects of different PEEP levels with or without scheduled recruiting maneuvers in patients undergoing general anesthesia for open abdominal surgery and receiving low-tidal volume ventilation.

NCT ID: NCT02986269 Completed - Anesthesia, General Clinical Trials

PSV on Ventilation Inhomogeneity and Lung Function in Patients Under SB Across LMA

VINHO
Start date: April 13, 2018
Phase: N/A
Study type: Interventional

General anesthesia has been demonstrated to have a negative impact on lung function. Both surgery and patient position influence the perioperative lung function. Laryngeal mask airway (LMA) has been proved to be safe and efficient to maintain the airways patent during general anesthesia. Pressure support ventilation (PSV) with LMA is routinely used in clinical practice. The aim of the present trial is to characterize perioperative changes in lung volume, ventilation inhomogeneity and respiratory mechanics in patients in the lithotomy position and spontaneously breathing through LMA with and without PSV.

NCT ID: NCT02955680 Completed - Anesthesia, General Clinical Trials

Recorded Maternal Voice on the Emergence of General Anesthesia on Pediatric Patients

Maternal voice
Start date: November 2016
Phase: N/A
Study type: Interventional

Mother spend a large amount of time with their children. It is assumed that mother contributes to their neurological development not only with visual stimuli, but also with auditory stimuli. A recent study revealed that prefrontal cortex can be activated in response to the self-name being spoken by the mother than by a stranger. Therefore, investigators suppose that recorded maternal voice can stimulate the pediatric patients and thereby fasten the emergence from general anesthesia.

NCT ID: NCT02930096 Completed - Anesthesia General Clinical Trials

Study of the Effect of the Supine Position at Brain Velocities in Noncerebro - Injured Patient

D-Velocity
Start date: March 2016
Phase:
Study type: Observational

To evaluate the pulsatility index changes after setting supine position in non brain- injured patient under general anesthesia.

NCT ID: NCT02860377 Completed - Anesthesia, General Clinical Trials

Maternal Voice on Anesthetic Emergence Period

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

Mother spend a large amount of time with their children. It is assumed that mother contributes to their neurological development not only with visual stimuli, but also with auditory stimuli. A recent study revealed that prefrontal cortex can be activated in response to the self-name being spoken by the mother than by a stranger. Therefore, investigators suppose that recorded maternal voice can stimulate the pediatric patients and thereby fasten the emergence from general anesthesia.

NCT ID: NCT02714777 Completed - Anesthesia, General Clinical Trials

General Anesthesia and Autonomic Nervous System in Children

ANESPEDIA
Start date: June 2016
Phase: N/A
Study type: Observational

The objective of the ANESPEDIA study is to describe in a pediatric population (aged from 4 to 8 years old) receiving elective surgery, the impact of general anesthesia on autonomic nervous system and their kinetics of early postoperative course (24 hours).

NCT ID: NCT02711280 Completed - Anesthesia, General Clinical Trials

The Effect of Anesthetics on Oxidative Stress and Apoptosis Status in Children

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

The purpose of this study is to determine whether Propofol and Sevoflurane affect the oxidative stress and apoptosis status in children undergoing hypospadias repair surgery.