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Residual Neuromuscular Blockade clinical trials

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NCT ID: NCT05992090 Recruiting - Clinical trials for Neuromuscular Blockade

Neuromuscular Blockade Monitoring Using Kine-myography vs Electromyography.

Start date: October 10, 2023
Phase:
Study type: Observational

This study aims to compare two monitoring methods of neuromuscular blockade - Kine-myography and Electromyography. The main questions to answer are: - are electromyography and kine-myography interchangeable - is electromyography linked to fewer fault results - is electromyography using lower energy to stimulate nerves The type of study is a multicentric observational clinical trial. Subjects are patients undergoing general anaesthesia with the use of rocuronium or cis-atracurium. In each patient, the neuromuscular blockade will be monitored using kine-myograph and electromyography simultaneously.

NCT ID: NCT04619225 Enrolling by invitation - Clinical trials for Residual Neuromuscular Blockade

Cardiac Output and Recovery Time

Start date: September 14, 2022
Phase: N/A
Study type: Interventional

The purpose of this research is to determine the time it takes to reverse the effects of the intraoperative medication given to relax the muscles and how this period of recovery correlates with a function of the heart.

NCT ID: NCT04352140 Completed - Clinical trials for Residual Neuromuscular Blockade

Electromyographic and Acceleromyographic Monitoring in Restricted Arm Movement Surgical Setting

Start date: August 18, 2020
Phase: N/A
Study type: Interventional

Researchers are comparing the ease of use and repeatability of the force vs electrical activity produced by a muscle after it has undergone nerve stimulation during a surgical procedure in which the patients' arm movement is restricted (placed under surgical drapes) in laparoscopic or robotic procedures.

NCT ID: NCT04352127 Completed - Clinical trials for Residual Neuromuscular Blockade

Visual and Electromyography Assessments in Response to Train-of-Four Stimulation of the Ulnar Nerve

Start date: August 18, 2020
Phase: N/A
Study type: Interventional

Researchers are comparing the accuracy of measuring muscle relaxation during and after surgery with a device that provides numeric value versus visual observation to count of muscle twitches or absence of them by a medical provider monitoring your anesthesia during surgery.

NCT ID: NCT04312256 Completed - Clinical trials for Residual Neuromuscular Blockade

Thumb vs Great Toe Recovery

Start date: August 18, 2020
Phase: N/A
Study type: Interventional

Researches are comparing the accuracy of measuring muscle relaxation in the thumb versus the great toe.

NCT ID: NCT04244266 Completed - Obesity Clinical Trials

Observational Study in Bariatric Surgery

NEOCURE
Start date: January 29, 2020
Phase:
Study type: Observational

Obesity in the world represents a growing share of the general population. At hospital, the management of these patients could be problematic especially when calculating the drug dosage. According to the French guidelines, neostigmine, a cholinesterase inhibitor, should be used to reverse a residual neuromuscular blockade at a dose of 0.4 mg/kg of total body weight in non-obese patients. In morbidly-obese patients, with the modification of the fat/lean mass ratio, the optimal dose of neostigmine is non-consensual. To calculate the dose of neostigmine, some anesthesiologists use the total body weight, others use the ideal body weight and others use the adjusted body weight. Due to this practice variability, It may be useful to observe the mean time to recovery of neuromuscular blockade and side effects after pharmacological reversal according to the dosage of neostigmine.

NCT ID: NCT03920670 Completed - Clinical trials for Residual Neuromuscular Blockade

Comparison of the ToFscan and TetraGraph During Recovery of Neuromuscular Function in the Post Anesthesia Care Unit

Start date: February 28, 2019
Phase: N/A
Study type: Interventional

The aim of this investigation is to compare the performance of two quantitative monitors utilized on post-anesthesia recovering patients. The ToFscan (Draeger Medical Inc., Telford, PA) represents one of the few standalone acceleromyography (AMG)-based quantitative monitors available for routine clinical use in the United States. The TetraGraph (Senzime AB, Uppsala, Sweden) is a standalone electromyography (EMG)-based quantitative monitor that recently received Conformité Européene (CE) approval. While both of these quantitative monitors can be utilized to guide intraoperative NMBA re-dosing and confirm recovery, they provide their objective data via drastically different techniques.

NCT ID: NCT03585400 Completed - Clinical trials for Residual Neuromuscular Blockade

Validation of the REPS Prediction Tool

Start date: June 29, 2018
Phase:
Study type: Observational

Neuromuscular blocking agents' (NMBA) use during surgery is associated with postoperative respiratory complications and increased risk of readmission to the hospital following ambulatory surgery. Residual neuromuscular block (rNMB) after surgery is difficult to identify. We have recently developed the REsidual neuromuscular block Prediction Score (REPS), that predicts the risk for postoperative rNMB. Our primary objective is now to assess the predictive ability of the REPS for respiratory complications within seven days following general anaesthesia. The secondary objective is to compare the predictive values of REPS and train-of-four (TOF)-ratio below 0.90 for respiratory complications.

NCT ID: NCT03574337 Withdrawn - Clinical trials for Residual Neuromuscular Blockade

Residual Neuromuscular Blockade in Cardiac Surgery Patients

Start date: August 1, 2018
Phase: Phase 4
Study type: Interventional

The purpose of this project is to determine if reversal of neuromuscular blockade in cardiac surgery patients expedites time to extubation in fast track patients.

NCT ID: NCT03417804 Completed - Clinical trials for Neuromuscular Blockade

Incidence of Postoperative Residual Neuromuscular Blockade in Portugal

Start date: June 18, 2018
Phase:
Study type: Observational

This is an epidemiological multicenter, observational, prospective study, designed to determine the incidence of postoperative residual neuromuscular blockade - defined by a TOF (train-of-four) ratio < 0.9 - at PACU arrival. Subjects aged at least 18 years old (n=360) admitted for different types of elective surgical procedures requiring general anesthesia with neuromuscular blocking agents will be included.