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Postoperative Delirium clinical trials

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NCT ID: NCT05596071 Completed - Clinical trials for Postoperative Delirium

Whether Opioids Are Factor That Induced POD?

POD
Start date: June 25, 2016
Phase: N/A
Study type: Interventional

The purpose of this study was to investigate whether perioperative use of low doses of opioids could reduce postoperative delirium .

NCT ID: NCT05548153 Completed - Clinical trials for Postoperative Delirium

An Observational Study on the Relationship Between Tear Metabolomics and POD

Start date: August 22, 2022
Phase:
Study type: Observational

To explore the correlation between tear metabolomics and POD. The purpose of this study was to compare the results of tear metabolomics between POD and non-POD elderly patients undergoing abdominal surgery, to clarify the correlation between tear metabolomics and POD, and to find tear markers related to POD.

NCT ID: NCT05466279 Completed - Clinical trials for Postoperative Delirium

The Role of Remazolam in Reducing the Incidence of Postoperative Delirium in Elderly Patients

Start date: January 7, 2021
Phase: N/A
Study type: Interventional

This study is a prospective, randomized, controlled trial.The selected patients were randomly divided into remazolam general anesthesia group and propofol + midazolam general anesthesia control group according to computer randomization method. There were 65 patients in each group. Remazolam general anesthesia group (R group): Remazolam 0.4 mg/kg for rapid induction of loss of consciousness for anesthesia induction and 1 mg/kg/h for maintenance. Propofol + midazolam general anesthesia control group (group P): propofol 1.5 mg/kg + midazolam 0.05 mg/kg slow intravenous push until the patient's consciousness disappeared, then propofol 4-8 mg/kg/h Anesthesia was maintained. Except for different sedative drugs, the analgesic and muscle relaxant medication regimens were the same between the two groups. In the study, the application of inhaled anesthetics, other benzodiazepines and anticholinergic drugs was restricted, and the mean arterial pressure during the operation was kept above 60 mmHg to avoid perioperative hypotension, hypoxemia, and hypercapnia. Warm measures were used to maintain the patient's intraoperative body temperature above 36.0 °C. POD assessment was performed on the day before surgery and on days 1-7 after surgery.

NCT ID: NCT05457387 Completed - Clinical trials for Postoperative Delirium

Relationship Between Perioperative Sleep Disturbance and Postoperative Delirium

Start date: April 1, 2020
Phase:
Study type: Observational

The investigators are performing this research study to understand the role of sleep disturbance on the incidence of delirium after surgery.

NCT ID: NCT05456230 Completed - Clinical trials for Postoperative Delirium

Comparison of Postoperative Delirium in Elders Anaesthetised With Midazolam and Without Midazolam

Start date: April 1, 2020
Phase:
Study type: Observational

This research project is an observational cohort study by prospective chart review of patients that underwent surgery in multi-centers, China, in the years 2020-2022. The purpose of this study is to compare the occurrence of postoperative delirium With Midazolam and Without Midazolam During Non-cardiac Surgery in Elders.

NCT ID: NCT05368272 Completed - Clinical trials for Postoperative Delirium

EEG Spectrogram, Brain Vulnerability and POD

Start date: January 27, 2023
Phase:
Study type: Observational

An assessment of difference in prespecified processed electroencephalography variables between cognitively intact older surgical patients who develop postoperative delirium compared to those who do not develop postoperative delirium

NCT ID: NCT05331027 Completed - Clinical trials for Postoperative Delirium

The Effect of Desflurane Versus Sevoflurane on Postoperative Recovery

RAPID
Start date: May 1, 2022
Phase: Phase 4
Study type: Interventional

Patients over the age of 65 years are at increased risk for developing delirium and cognitive complications in the immediate postoperative period after noncardiac surgeries, resulting in increased morbidity and mortality. Previous small studies have shown beneficial effects of desflurane on postoperative cognitive recovery, which has been explained by the more rapid onset and offset of anesthesia as compared to sevoflurane. However, there are very limited data on the effect of desflurane on postoperative recovery and time until criteria for discharge from post-anesthesia care unit (PACU) are fulfilled in elderly patients undergoing minor-to moderate-risk noncardiac surgery. Therefore, the investigators will test the primary hypothesis that general anesthesia with desflurane significantly reduces the time between discontinuation of volatile anesthetics after the end of surgery and reaching ready for discharge from PACU criteria, which are defined as reaching a modified Aldrete score ≥ 12, as compared to sevoflurane in patients ≥ 65 years of age undergoing minor-to moderate-risk noncardiac surgery.

NCT ID: NCT05209555 Completed - Clinical trials for Cognitive Impairment

Preoperative BAMCOG and Cortisol and Postoperative DeltaScan in AVR Patients (Aortic Valve Replacement)

Start date: January 10, 2022
Phase:
Study type: Observational

There is lack of attention to preoperative cognitive function and delirium in elderly who underwent surgery. The investigators are investigating different tools that can help to screen for cognitive dysfunction and delirium in the future.

NCT ID: NCT04987372 Completed - Postoperative Pain Clinical Trials

Multimodal Versus Opioid aNalgesia in carDiAc Surgery

MONDAY
Start date: January 21, 2019
Phase: Phase 4
Study type: Interventional

To compare standard "Fentanyl - Tramadol - Paracetamol - Oxycodone" regimen to a multimodal painmanagement "pregabalin- minimal fentanyl-ketamine-lidocain-dexmedetomidine- paracetamol" to determine which therapy provides the most comfort, the fastest extubation time, the least pain and the least delirium.

NCT ID: NCT04820595 Completed - Clinical trials for Postoperative Delirium

Postoperative Neurocognitive Dysfunction: Is There Any Place for Emergency Agitation: A Prospective Cohort Trial

PoD
Start date: March 30, 2021
Phase:
Study type: Observational

Perioperative neurocognitive disorders (PND) have been studying by clinicians, particularly by anesthesiologists, pretty long, however the most inspiring advancements were achieved during the last few decades. The most recent classification of PND which includes cognitive decline diagnosed before operation (described as neurocognitive disorder); any form of acute event (postoperative delirium) and cognitive decline diagnosed up to 30 days after the procedure (delayed neurocognitive recovery) and up to 12 months (postoperative neurocognitive disorder) was proposed in 2017. However at will one can notice at least one uncertainty that pertinent to the definition of delirium, emergency delirium and not mentioned in the classification discussed agitation. The objective of the study is to determine if there is a difference between emergence agitation and emergence delirium.