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Emergence Delirium clinical trials

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NCT ID: NCT02720705 Completed - Agitation Clinical Trials

Transbucal Dexmedetomidine for Prevention of Sevoflurane Emergence Agitation in Pre-school Children

Start date: May 2016
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this study is to evaluate the efficacy of transbucal dexmedetomidine given in preschool children undergoing tonsillectomy operations in the prevention sevoflurane agitation.

NCT ID: NCT02692300 Completed - Clinical trials for Post-operative Delirium

EEG Guidance of Anesthesia (ENGAGES-CANADA)

ENGAGES
Start date: December 28, 2016
Phase: N/A
Study type: Interventional

This study examines the potential link between deep levels of anesthesia and delirium.

NCT ID: NCT02585128 Completed - Clinical trials for Postoperative Delirium

Predictors of Postoperative Delirium After Transcatheter Aortic Valve Implantation

Start date: September 2015
Phase: N/A
Study type: Interventional

Patients undergoing transcatheter aortic valve implantation (TAVI) have distinctive characteristics: they are old, frail, with several co-morbidities and take multiple medications. Hemodynamic instability, cerebral embolism, sedation, general anesthesia and hospitalization in intensive care expose those patients to postprocedural delirium. Acute neurocognitive dysfunctions are associated with adverse outcomes in these population. The objective of this study is to determine the incidence of delirium and neurocognitive disorders in elderly patients after TAVI.

NCT ID: NCT02521259 Completed - Strabismus Clinical Trials

Anesthetic Depth and the Incidence of Emergence Agitation in Children Undergoing Strabismus Surgery

Start date: April 2015
Phase:
Study type: Observational

This study evaluates the association between the depth of general anesthesia and the occurrence of emergence agitation (EA). The investigators hypothesized that optimal level of anesthetic depth could decrease the incidence of EA in children undergoing strabismus surgery compared to the deep level of anesthetic depth.

NCT ID: NCT02509221 Completed - Clinical trials for Delirium on Emergence

Effect of Duration of Exposure of Anesthesia With Sevoflurane on Emergence Delirium

Start date: July 2015
Phase:
Study type: Observational

Emergence delirium which is a phenomenon seen commonly in preschool kids anesthetized with Sevoflurane. Restless recovery from anesthesia may not only cause injury to the child or to the surgical site, but may also lead to the accidental removal of surgical dressings, IV catheters, and drains. is one of the The purpose of the study is to find whether duration of exposure to Sevoflurane has any effect on the incidence of Emergence Delirium.

NCT ID: NCT02489734 Completed - Clinical trials for Delirium on Emergence

Post Extubation Delirium and End-tidal Sevoflurane Concentration

Start date: July 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the incidence of emergence delirium will be reduced when end-tidal concentration of sevoflurane decreases.

NCT ID: NCT02325154 Completed - Clinical trials for Post-operative Delirium

Cerebral Oxygenation in Total Hip Arthroplasty Patients

THANIRS
Start date: December 2014
Phase: N/A
Study type: Interventional

We plan to investigate the relationship between hypotensive epidural anesthesia for hip arthroplasty and cerebral oxygen saturation.

NCT ID: NCT02213380 Completed - Clinical trials for Post Operative Delirium

Effect of Anesthesia on Post-operative Delirium in Elderly Patients Undergoing Hip Fracture Surgery

RAGADelirium
Start date: September 2014
Phase: N/A
Study type: Interventional

The purpose of this study is evaluate postoperative delirium after general anesthesia and regional anesthesia in elderly patients undergoing hip fracture surgery. Our research hypotheses are: (1) regional anesthesia may contribute to decrease the incidence of postoperative delirium. (2) Regional anesthesia may improve the outcome of elderly patient and reduce healthcare costs associated with postoperative delirium. (3) Postoperative delirium may result in poor long-term functional outcomes.

NCT ID: NCT01535287 Completed - Myringotomy Clinical Trials

Effect of Dexmedetomidine on Emergence Agitation in Children With or Without Tube Insertion Under General Anesthesia

Start date: January 4, 2011
Phase: Phase 4
Study type: Interventional

The investigators are inviting your child to participate in this research study because your child is having myringotomy (putting a tiny incision in the eardrum with or without tube insertion) under general anesthesia. The purpose of this study is to determine whether a single injection of Dexmedetomidine (study medication) decreases the frequency of awaking from anesthesia frightened or agitated in children having myringotomy surgery as compared to those children who receive placebo (sterile saltwater).

NCT ID: NCT01528891 Completed - Tonsillectomy Clinical Trials

Dexmedetomidine as a Rapid Bolus in Children for Emergence Agitation

Start date: January 2012
Phase: Phase 3
Study type: Interventional

To Determine The Efficacy of a Rapid Bolus Injection of Dexmedetomidine on the Incidence of Emergence Agitation in Anesthetized Children and the Cardiovascular Profile of a Rapid Bolus Injection of Dexmedetomidine.