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Anesthesia; Adverse Effect clinical trials

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NCT ID: NCT04604106 Recruiting - Anesthesia Clinical Trials

General Anesthesia Exposure and Neurodevelopmental Outcome in Pediatrics

GAP
Start date: October 21, 2020
Phase:
Study type: Observational

This study investigates the impact of different levels of anesthesia exposure on children's neurocognitive development and evaluates the concurrent validity of different methods that assess neurodevelopmental outcome.

NCT ID: NCT04455776 Completed - Clinical trials for Sedation Complication

Safety Evaluation of Propofol Sedation for Magnetic Resonance Imaging in Pediatric Patients

Start date: July 3, 2020
Phase:
Study type: Observational

Propofol is often used for sedation in children undergoing magnetic resonance imaging. The investigators will perform a chart review of 4 month of activity (about 100 cases) and review the incidence and severity of adverse events of this sedation technique.

NCT ID: NCT04377633 Recruiting - Clinical trials for Postoperative Complications

Anesthesia-handover Checklist and Perioperative Outcomes in Elderly

Start date: July 16, 2020
Phase: N/A
Study type: Interventional

With the increasing number of surgical cases, intraoperative handover of anesthesia care is common and inevitable. Verbal handover from one anesthesiologist to another during surgery are being used in many hospitals. However, verbal handover is often an informal, unstructured process during which omissions and errors can occur. It is possible that an improved anesthesia handover may reduce the related adverse events. This study aims to test the hypothesis that use of a well-designed, structured handover-checklist to improve handover quality may decrease the occurrence of postoperative complications in elderly patients undergoing major noncardiac surgery.

NCT ID: NCT04322994 Enrolling by invitation - Clinical trials for Anesthesia; Adverse Effect

THRIVE Use in Pediatric Populations- Multi Site

Start date: October 21, 2020
Phase: N/A
Study type: Interventional

THRIVE (Transnasal Humidified Rapid-Insufflation Ventilatory Exchange) refers to the use of high-flow nasal cannula to augment the ability to oxygenate and ventilate a patient under general anesthesia. The use of high-flow nasal cannula oxygen supplementation during anesthesia for surgical procedures has been a recent development in the adult population, with limited data analyzing the pediatric population. This study will determine whether high flow nasal cannula oxygen supplementation during surgical or endoscopic procedures can prevent desaturation events in children under anesthesia and improve the outcomes of that surgery.

NCT ID: NCT04284644 Completed - Anesthesia Clinical Trials

Co-induction Technique Compared to Standard Inhalational and Intravenous Induction Techniques

Start date: May 1, 2016
Phase: N/A
Study type: Interventional

Co-induction technique refers to the use of a combination of medications to reach the desired therapeutic target. In the present study, the investigators examined the safety of a novel co-induction approach that relied on a simple timing and dosing alterations to the classical approaches of inhalational sevoflurane and propofol induction. The significance of this study is to find a reliable safe alternative method of induction that can provide optimal parameters,when compared to the classical methods of induction.

NCT ID: NCT04275531 Active, not recruiting - Clinical trials for Anesthesia; Adverse Effect

Neurotoxicity of Anesthesia in Middle Aged Patients

Start date: March 1, 2021
Phase:
Study type: Observational

for the last 20 years, the increasing reports from non-human studies have raised suspicion that general anesthetics may cause neurotoxic changes in the developing brain that lead to adverse neurodevelopmental outcomes later in life.there are several case reports of reversible smell and taste dysfunction following exposure to general anesthesia suggesting a possible relationship between anesthetic agents and olfactory dysfunction. this study is to assess the possible neurotoxicity of sevoflurane,isoflurane,and propofol based anesthesia guided by olfactory changes

NCT ID: NCT04178200 Not yet recruiting - Anesthesia, Local Clinical Trials

Evaluation of Duration of Anesthesia and Patient Satisfaction After Retrobulbar Block Applied in Cataract Surgery

Start date: December 16, 2019
Phase:
Study type: Observational

It is aimed to determine patient satisfaction (pain assessment during and after the operation) and the initial and total anesthesia durations of eye lid and globe anesthesia after administration of local anesthetic solution only in standard applied volumes (1.5-3 ml). No agents will be added to the local anesthetic agents used in the conventional retrobulbar block in patients who will undergo cataract surgery,

NCT ID: NCT04087668 Completed - Clinical trials for Anesthesia; Adverse Effect

Different Anesthetic Technique For ERCP

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

Providing the appropriate anesthetic technique for endoscopic retrograde cholangiopancreatography (ERCP) in remote locations can be challenging. The aim of this study was therefore to prospectively assess and compare the feasibility of monitored anesthesia care (MAC) with propofol based deep sedation, standard general anesthesia and general anesthesia without neuromuscular blockade in patients undergoing ERCP.

NCT ID: NCT03967496 Completed - Delirium Clinical Trials

Assessment of Immediate Postoperative Delirium (IPD) in Adult Patients: Incidence and Etiologic Factors

AIPDAP
Start date: January 1, 2019
Phase:
Study type: Observational [Patient Registry]

Delirium is considered to be acute failure of central nervous system. It is acute confusional state characterized by decline from baseline mental level, attention deficit and disorganized thinking. Postoperative delirium is known to prolong length of stay in hospital, cause functional decline and dementia, increase all-cause mortality and increase the medical cost. It is also associated with other outcomes like cardiac arrest, ventricular tachycardia or fibrillation, myocardial infarction, pulmonary edema, pulmonary embolism, bacterial pneumonia, respiratory failure requiring intubation, renal failure requiring dialysis and stroke. There are well known predisposing and precipitating factors related to its etiology. However, the effect of type of anesthesia is not very clear. There have been no major clinical trials in this part of the world to delineate the incidence of immediate postoperative delirium (IPD). The investigators have undertaken this prospective observational study to determine the incidence of IPD and its etiological factors in adult patients during their stay in the Post-Anesthesia Care Unit (PACU) following surgery under different types of anesthesia (general anesthesia, regional anesthesia and monitored anesthesia care). The study was done over a period of about three months. Assessment for delirium was done using Confusion Assessment Method-Intensive Care Unit (CAM-ICU score, English/Arabic version). Sedation and Agitation were assessed using Richmond Agitation Sedation Score (RASS). Pain was assessed using Numeric Pain Score (NPS). Assessment was done within 24 hours prior to surgery and was repeated at three different intervals in PACU. Details of perioperative management were recorded and analyzed. The incidence of IPD and its etiologic factors were identified thereby leading to corrective action.

NCT ID: NCT03882788 Completed - Clinical trials for Congenital Heart Disease

The Effect of Anesthesia on Neurodevelopmental Outcome (NDO)

NDO
Start date: April 22, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether the type of anesthesia, narcotic-based versus inhalational anesthesia administered during cardiopulmonary bypass (CPB) surgery contributes to the wide variation in neurologic recovery and developmental outcome after surgery in infants with congenital heart disease.