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Anesthesia clinical trials

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NCT ID: NCT03643913 Recruiting - Anesthesia Clinical Trials

The Effect of Deep Neuromuscular Block and Reversal With Sugammadex on Surgical Conditions and Perioperative Morbidity in Shoulder Surgery Using a Deltopectoral Approach

Start date: December 18, 2018
Phase: Phase 4
Study type: Interventional

The study evaluates wether deep neuromuscular block during entire surgical procedure to the gleno-humeral joint or the proximal humerus using a deltoideo-pectoral approach results in less muscular damage to the deltoid muscle and therefore less post-operative pain and an earlier functional recovery..

NCT ID: NCT03642301 Completed - Anesthesia Clinical Trials

Dosing of Carcinogenic Complexes After Anesthesia With Intrathecal Hyperbaric Prilocaine.

Start date: January 10, 2019
Phase:
Study type: Observational

The prilocaine is a very common local anesthetic that has the disadvantage of being metabolized to o-toluidine, a human carcinogen. Hyperbaric 2% prilocaine (HP), recently developped, is increasingly used for spinal anesthesia in ambulatory surgery. But the formation of carcinogenic metabolites induced by the hyperbaric prilocaine is not yet known. The aim of this study is to investigate whether the intrathecal administration of 50 mg hyperbaric prilocaine induces also the formation of carcinogenic complexes such as urinary o-toluidine and hemoglobin adducts from o-toluidine in blood.

NCT ID: NCT03640468 Not yet recruiting - Anesthesia Clinical Trials

Lidocaine as an Adjuvant for Ketamine in Induction of Anesthesia in Septic Shock Patients

Start date: December 20, 2018
Phase: Phase 3
Study type: Interventional

The aim of the work is to investigate the effect of using lidocaine in combination with low dose ketamine in induction of anesthesia for septic shock patients compared to normal dose of ketamine.

NCT ID: NCT03640442 Completed - Obesity Clinical Trials

Modified Ramped Position for Intubation of Obese Females.

Start date: September 9, 2018
Phase: N/A
Study type: Interventional

The aim of this work is to investigate the feasibility of using the modified a ramped position for intubation of obese females in comparison to the traditional ramped position.

NCT ID: NCT03629743 Active, not recruiting - Anesthesia Clinical Trials

Correlate of Surface Electroencephalogram (EEG) With Implanted EEG Recordings (ECOG)

Start date: November 11, 2019
Phase:
Study type: Observational

Improve understanding of the correlation between surface EEG and implanted EEG recordings

NCT ID: NCT03624166 Completed - Anesthesia Clinical Trials

Impact of Sub-anesthetic Dose of Ketamine on Post Spinal Hypotension in Caesarean Delivery

Start date: February 1, 2019
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the effect of sub anesthetic dose of ketamine on vasopressor (Ephedrine) requirement to prevent maternal hypotension after spinal anesthesia in caesarean section.

NCT ID: NCT03620942 Active, not recruiting - Anesthesia Clinical Trials

Development of Advanced Double Intravenous Vasopressor Automated (ADIVA) System

ADIVA
Start date: November 7, 2018
Phase: N/A
Study type: Interventional

Maternal hypotension during spinal anaesthesia for Caesarean delivery may bring various adverse effects. It is therefore important to closely monitor hypotension during spinal anaesthesia, however current technology does not allow the blood pressure monitoring to respond in timely manner should there be any occurrence of hypotension. The investigators developed an advanced double-intravenous vasopressor automated system (ADIVA) so as to tackle this issue via novel algorithm to control blood pressure more rigorously with more stable haemodynamic profiles.

NCT ID: NCT03615417 Completed - Obesity Clinical Trials

High-Flow Nasal Cannula (HFNC) Preoxygenation in Obese Patients Undergoing General Anesthesia

Start date: April 19, 2018
Phase: N/A
Study type: Interventional

This study aims to evaluate the effectiveness of the High Flow Nasal Cannula (HFNC) for the preoxygenation of obese patients undergoing a general anesthesia. The HFNC interface is compared to a standard anesthesia FaceMask (FM) preoxygenation with Continuous Positive Airway Pressure (CPAP), the current gold standard procedure for obese induction. The interest of HFNC preoxygenation is to increase the "safe apnea time" before critical arterial desaturation, useful in the management of difficult airways, especially in subjects with reduced respiratory reserves such as the obese.

NCT ID: NCT03610282 Withdrawn - Anesthesia Clinical Trials

EEG Study of IV Methylphenidate-Induced Emergence From Propofol Sedation

Start date: November 2019
Phase: Phase 1/Phase 2
Study type: Interventional

The investigators are performing this research study to find out if intravenous (IV) methylphenidate (commonly known as Ritalin) can help people recover faster from propofol sedation. The investigators also want to know how IV methylphenidate acts in the brain and whether IV methylphenidate is safe to take with an anesthetic (a drug or agent used to decrease or eliminate the feeling of pain by causing unconsciousness) without causing too many side effects. The brain's electrical activity will be studied and recorded using a machine called an electroencephalogram (EEG).

NCT ID: NCT03600727 Not yet recruiting - Anesthesia Clinical Trials

Propofol and Dexmedetomidine on Inflammation

Start date: August 2018
Phase: N/A
Study type: Interventional

Dexmedetomidine, was reported to prevent postoperative delirium in elderly patients following its use in intensive care units. Possible mechanisms included improved quality of sleep and an inhibitory effect on inflammation. A greater number of studies indicated that propofol has negative effect on postoperative cognitive function. In this study, we planned to investigate the influence of these two different sedative drugs on peripheral inflammation induced by surgery and postoperative cognitive function of patients who will receive hip and knee arthroplasty.