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Postoperative Delirium clinical trials

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NCT ID: NCT05168280 Recruiting - Clinical trials for Postoperative Delirium

Intraoperative Infusion of Dexmedetomidine for Prevention of Postoperative Delirium in Elderly Patients

Start date: July 18, 2022
Phase: N/A
Study type: Interventional

Postoperative delirium (POD) is a common surgical complication. The incidence is 10% to 22% in neurological procedures, and advanced age is a risk factor for neurological procedures. Many studies have shown that dexmedetomidine(DEX) may reduce the incidence of delirium in non-cardiac surgery patients and elderly patients. However, there are few studies focus on the effect of DEX on POD in elderly patients undergoing neurosurgery. The purpose of this study was to investigate the effect of DEX on POD in in elderly patients undergoing craniotomy.

NCT ID: NCT05164965 Not yet recruiting - Clinical trials for Postoperative Delirium

C-reactive Protein,Homocysteine,Postoperative Delirium

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

The aim of this study is to evaluate how C-reactive protein (CRP) and homocysteine and their interaction contribute to postoperative delirium, based on our previous finding on the interactions of CRP, homocysteine and postoperative delirium.

NCT ID: NCT05140993 Recruiting - Clinical trials for Postoperative Delirium

The Role of Emotional and Orientation Support in Prevention of Postoperative Delirium Among Elderly Surgical Patients

Start date: June 1, 2022
Phase: N/A
Study type: Interventional

Postoperative delirium is common and associated with significant adverse outcomes. Its etiology is unknown, and little is known about associated risk factors. The investigatorea aim to test whether providing emotional and orientation support can reduce the risk of postoperative delirium in elderly patients undergoing elective non-cardiac surgery. Specifically, the investigators will test whether allowing such patients to keep their hearing and visual aids and be escorted into the operating room by a family member until anesthesia induction reduces the incidence of postoperative delirium. Delirium will be actively screened as part of our institution's clinical practice starting at PACU admission and for a minimum of 2 postoperative days. The investigators will use a multiple cross-over design to enroll all eligible patients and alternate between the intervention and our common practice (removing sensorial aids in the preoperative area and not allowing patients' escort beyond that point) every 2 weeks for up to 2 years.

NCT ID: NCT05096507 Recruiting - Clinical trials for Postoperative Delirium

Cytokines, POD, Health Status, Older Hip Fracture

Start date: June 6, 2022
Phase:
Study type: Observational

An investigation of the change in inflammation marker levels across hip fracture surgery and an exploration of any association with change in self reported health status and incidence of postoperative delirium

NCT ID: NCT05081726 Not yet recruiting - Hip Fractures Clinical Trials

fMRI Feasibility Older Hip Fracture Surgery

Start date: July 4, 2022
Phase:
Study type: Observational

An assessment of the feasibility of structural and functional magnetic resonance imaging (MRI) brain scans in older people who have recovered from and older people who never had delirium after hip fracture surgery

NCT ID: NCT05036538 Recruiting - Clinical trials for Postoperative Delirium

Decreasing Preoperative Stress to Prevent Postoperative Delirium and Postoperative Cognitive Decline in Cardiac Surgical Patients.

DESTRESS-SURG
Start date: July 27, 2023
Phase: N/A
Study type: Interventional

Patients undergoing cardiac surgery often complain of anxiety before a major operation and the resulting stress. This circumstance is a risk factor for mental problems that may occur after the operation (e.g., delirium or memory deficits). This study aims to prevent these discomforts by a preoperative relaxation intervention.

NCT ID: NCT05010148 Recruiting - Postoperative Pain Clinical Trials

A Clinical Trial of Intravenous Lidocaine After Spinal Surgery to Prevent Delirium and Reduce Pain

LIMPP
Start date: September 17, 2021
Phase: Phase 3
Study type: Interventional

Postoperative delirium is one of the most frequent adverse events following elective non-cardiac surgery and is associated with cognitive impairment at discharge, as well as in-hospital and long-term mortality, however, despite being a well-recognized problem there is a dearth of effective interventions for prevention and management. A modifiable risk factor associated with postoperative delirium is poor postoperative pain control, and by improving the pain regimen the investigators may be able to decrease the incidence and/or severity of postoperative delirium. In this study, the investigators seek to study whether a postoperative intravenous infusion of lidocaine, known to improve pain control in other contexts, can decrease the risk of postoperative delirium and other opioid-related side effects, following major reconstructive spinal surgery.

NCT ID: NCT05001425 Recruiting - Cardiac Surgery Clinical Trials

Association Between the Brain Excitability and Postoperative Delirium in Patients Undergoing Heart Valve Replacement Surgery With Cardiopulmonary Bypass

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

The purpose of this study is to explorethe brain excitability in patients undergoing heart valve replacement surgery with cardiopulmonary bypass and the correlation with postoperative delirium

NCT ID: NCT04999891 Recruiting - Hip Fractures Clinical Trials

The Southeast and East Asian Post-Operative Delirium (SEAPOD) Study

Start date: August 22, 2021
Phase:
Study type: Observational

The specific aim of the study will be to investigate the incidences and risk factors for postoperative delirium (POD) after hip fracture surgery in elderly patients aged ≥ 65 years in five different Southeast and East Asian countries. The secondary objectives are outlined below: 1. To investigate factors in the hospital environments, such as noise levels, ambient lighting, nursing ratios, ward bedding and climate control, that contribute to similarities and/or differences in POD occurrences in different countries and health systems 2. To investigate patient factors, such as disease burden, mental health, education levels, and socioeconomic factors, that contribute to similarities and/or differences in POD occurrences in different countries and health systems 3. To quantify the direct and indirect costs, as well as resource utilization, resulting from the development of POD in each country

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.