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Emergence Delirium clinical trials

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NCT ID: NCT05324852 Terminated - Emergence Delirium Clinical Trials

AGItated Patients Management: intraNASAL Midazolam vs Intramuscular Loxapine

AGINASAL
Start date: April 9, 2023
Phase: Phase 3
Study type: Interventional

This study is a non-inferiority phase III randomized trial evaluating the effect of intranasal midazolam versus intramuscular loxapine on the rapid tranquilization of agitated patient in emergency department. Intranasal midazolam is safe and may allow a management of extreme agitation state and prevent adverse effects.

NCT ID: NCT02604459 Terminated - Anesthesia Clinical Trials

Does Optimized General Anesthesia Care Reduce Postoperative Delirium?

OPCare
Start date: June 1, 2015
Phase: N/A
Study type: Interventional

Postoperative delirium occurs in up to 65% of elders undergoing surgery for repair of a hip fracture and this complication is independently associated with increased morbidity, mortality, length of hospital stay, and placement in long-term care institutions. To date, the only intervention shown to be effective at minimizing postoperative delirium is a proactive geriatric consultation. This prospective randomized clinical trial will randomize 160 adults, aged 65 years or older, to either optimized general anesthesia or usual general anesthesia care for hip fracture surgery to determine if the optimized anesthesia management reduces the severity of postoperative delirium.

NCT ID: NCT02111447 Terminated - Clinical trials for Delirium on Emergence

Post Anesthesia Emergence and Behavioral Changes in Children Undergoing MRI

Start date: January 2014
Phase: Phase 4
Study type: Interventional

Children who receive general anesthesia may become agitated (emergence delirium) in the recovery period. This occurs more often after inhalational anesthetics, particularly sevoflurane and desflurane than after propofol. However, agitation after anesthesia in children may be difficult to distinguish from pain; accordingly studies are ideally designed during MRI to obviate the contribution of pain during emergence. Airway complications have been reported after LMA and isoflurane more commonly than with IV propofol and nasal prongs. Whether the airway complications were due to the LMA or the isoflurane was unclear. Therefore, this study was designed to study the incidence of 1. agitation after sevoflurane compared with IV propofol and 2. airway complications after LMA or nasal prongs.

NCT ID: NCT00778063 Terminated - Otitis Media Clinical Trials

Study Using Dexmedetomidine to Decreases Emergence Delirium in Pediatric Patients

PED-DEX
Start date: September 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the use of intranasal dexmedetomidine to reduce the incidence of emergence delirium during general sevoflurane anesthesia in a pediatric population receiving pressure equalization tubes in one or more ear.