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Anesthesia clinical trials

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NCT ID: NCT04028284 Completed - Anesthesia Clinical Trials

HoloLens: an Objective Alternative to the Operator's Memory

Hololens
Start date: January 18, 2019
Phase: N/A
Study type: Interventional

Neuraxial anesthesia has traditionally been a 'blind' technique relying on users' feel and skill, both are subjective, lack complete accuracy and influenced by patient's physique variations that are quite challenging, and lead to patient morbidity, infection, and nerve injury. The ultrasound(US) use allows real-time views of needle position thereby achieving higher success rates, fewer complications, and reduced patient discomfort. While US guidance for neuraxial procedures is popular, it is still relatively uncommon due to technical and anatomical challenges. The study investigators have created an innovative methodology to use with HoloLens, an augmented reality tool, to provide an accurate live road map for the needle path hidden under the patient's skin. This see-through model is an objective alternative to the user's memory for direct visualization of the needle virtual trajectory as it passed through the tissue and towards the 3D printed bone. Also, this model may have a variety uses in anesthesia.

NCT ID: NCT04024904 Completed - Anesthesia Clinical Trials

Virtual Reality Hypnosis Distraction Utility to Improve Tolerance to Regional Anaesthesia

Start date: July 26, 2018
Phase: N/A
Study type: Interventional

Regional anaesthesia has many advantages but it might be a stressful and painful experience. Usually, the anesthetist administers a pharmacologic intravenous sedation to achieve patient's comfort. Though, these medications are not benign, and disadvantages include unpredictable response, adverse effects, and interference with cooperation. The virtual reality hypnosis distraction (VRHD) could be a good non-pharmacological technique to improve patient's comfort, decrease anxiety and procedure related pain. This study is a prospective study where sixty patients scheduled for orthopedic surgery requiring regional anesthesia were randomized in three groups according to the use or not of VRHD during the regional procedure or before as a complementary premedication. The anesthetic management during the regional procedure and the surgery remained otherwise standard for each patient. The first endpoint is the proportion of patients receiving pharmacological sedation (in the VRHD groups compared to the pharmacological sedation group). . The second endpoint is to determine if the VRHD increases the patient's satisfaction of their anaesthetic management. The third endpoint is to study various parameters of use of this specific anaesthetic management: time required for the installation and operation time of the VRHD device; the variation of haemodynamic parameters between the separate groups; pain procedure-related and behavioural pain scale scores between the separate groups.

NCT ID: NCT04024410 Completed - Surgery Clinical Trials

Optimal Positive End-expiratory Pressure (PEEP) in Prone Position During Spine Surgery

OPTIPRONE
Start date: June 3, 2019
Phase:
Study type: Observational

Background: There is a lack of studies regarding Optimal (best) positive end-expiratory pressure (PEEP) in prone position during surgery, and its relation with optimal PEEP in supine position. Hypothesis: In patients undergoing scheduled spinal surgery, optimal PEEP in the prone position is lower than optimal PEEP in the supine position. Aims: To assess the difference optimal PEEP in supine vs. prone positions in patients undergoing spine surgery. To evaluate the changes in optimal PEEP in prone position throughout the surgical procedure. Methods: Observational study, one center. Main variable: optimal PEEP. Secondary variables: PaO2, pCO2 and dynamic compliance (Crd) in prone and supine position.

NCT ID: NCT04020900 Completed - Anesthesia Clinical Trials

Respiratory Management of Children Under Anaesthesia

PEDIAVENT
Start date: June 21, 2017
Phase:
Study type: Observational

Ventilation management in paediatric anaesthesia remains difficult because of the wide range of age and weight, and therefore practices are heterogeneous. In adults, protective ventilation during anesthesia is now a standard of care but in children there is no level of evidence to recommend it. The aim of the study was to describe current practice and the factors associated with the use of high tidal volume during anaesthesia in children in France.

NCT ID: NCT04016454 Completed - Anesthesia Clinical Trials

Impact of Handover of Anesthesia Care on Adverse Postoperative Outcomes

HandiCAP
Start date: June 21, 2019
Phase: N/A
Study type: Interventional

Our goal is to conduct a prospective, national, randomized-controlled, multicenter trial to investigate the effect of handover of anesthesia care on the occurrence of adverse outcomes in the perioperative period.

NCT ID: NCT04014010 Completed - Surgery Clinical Trials

Machine Learning Modeling of Intraoperative Hemodynamic Predictors of Postoperative Outcomes

Start date: January 1, 2013
Phase:
Study type: Observational

With population aging and limited resources, strategies to improve outcomes after surgery are ever more important. There is a limited understanding of what ranges of hemodynamic variables under anesthesia are associated with better outcomes. This retrospective cohort study will analyze how hemodynamic variables during surgeries predict mortality, morbidity, Intensive Care Unit admission, length of hospital stay, and hospital readmission. The use of machine learning in a large, broad surgery population dataset could detect new relationships and strategies that may inform current practice, and generate ideas for future research.

NCT ID: NCT03984032 Completed - Anesthesia Clinical Trials

LMA Protector Cuff Pilot vs LMA Supreme Among Anaesthetised, Non-Paralysed Patients

Start date: July 17, 2018
Phase: N/A
Study type: Interventional

Comparison of clinical performance between LMA Protector Cuff Pilot and LMA Supreme in terms of oropharyngeal leak pressure, time to insertion, ease of gastric tube insertion, laryngeal view, incidence of sore throat

NCT ID: NCT03972423 Completed - Anesthesia Clinical Trials

Impact of a Transmission Checklist in Post Anesthesia Care Unit on Immediate Respiratory Complications

TC-IRC
Start date: February 18, 2019
Phase:
Study type: Observational [Patient Registry]

This work highlighted the beneficial role in terms of carers' satisfaction, quantity and quality of information transmitted.

NCT ID: NCT03970291 Completed - Anesthesia Clinical Trials

Impact of NOL Intraoperative Guided Fentanyl Analgesia vs SCC for Elective Major Abdominal Surgery

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

Recently, a newly developed index, the Nociceptive Level (NOL) index, was validated and showed superiority over heart rate and blood pressure for recognition and grading of intense and mild nociceptive stimuli during surgery under general anesthesia. We hypothesize that compared with standard management, NOL-guided anesthesia will lead to reduced postoperative pain scores, and during anesthesia, to increased hemodynamic stability.

NCT ID: NCT03963063 Completed - Anesthesia Clinical Trials

Neurological Effects of Goal-directed Fluid Therapy in Beach Chair Position Shoulder Surgery

Start date: June 27, 2019
Phase: N/A
Study type: Interventional

Patients receiving beach chair position shoulder surgery are vulnerable to perioperative cerebral desaturation, which is reported to be a risk factor for postoperative cognitive dysfunction. Investigators design this study to test the efficacy of perioperative goal-directed therapy in preventing cerebral desaturation and postoperative cognitive dysfunction in patients receiving beach chair position shoulder surgery.