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Delirium clinical trials

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NCT ID: NCT05069428 Recruiting - Delirium Clinical Trials

Delirium Reduction With Ramelteon

DREAM
Start date: March 26, 2023
Phase: Phase 4
Study type: Interventional

The overall purpose of this study is to identify a medication that might treat and/or prevent delirium in intensive care unit (ICU). Currently, there is no proven medical therapy for prevention or treatment of delirium. Ramelteon is a medication approved for insomnia. We hypothesize that ramelteon may help regulate the day/night cycle and decrease ICU delirium.

NCT ID: NCT05068180 Recruiting - Prostatic Neoplasms Clinical Trials

Low-dose Neuroleptanalgesia for Postoperative Delirium in Elderly Patients

Start date: October 5, 2021
Phase: Phase 4
Study type: Interventional

Postoperative delirium(POD)is a common complication that can directly affect important clinical outcomes, and exert an enormous burden on patients, their families, hospitals, and public resources. In order to evaluate whether an intraoperative administration of low-dose neuroleptanalgesia reduces postoperative delirium, droperidol 1.25 mg and fentanyl 0.025 mg or normal saline is used by intravenous injection 30 minutes before the end of the operation, in elderly patients with non-cardiac major surgery under general anesthesia. The efficiency and safety of neuroleptanalgesia on the incidence of POD would be evaluated in elderly patients.

NCT ID: NCT05066503 Recruiting - Subacute Delirium Clinical Trials

Nutritional Therapy for Delirium in Elderly Hospitalized Subjects

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

The investigators have developed a proprietary blend of amino acids that they think will help to prevent or reduce the severity of delirium in older people who are hospitalized for certain infections. In this study, up to 45 people will be enrolled. 15 will be asked to drink this blend twice a day for up to 4 days, and 15 will drink a placebo (sugar water) for the same time period. The other 15 subjects will be non-delirious control subjects who do not consume any study products.

NCT ID: NCT05060614 Recruiting - Delirium Clinical Trials

Analyses of Cerebrospinalfluid in Patients With Delirium

Start date: September 1, 2016
Phase:
Study type: Observational

The current project aims to measure biomarkers in the cerebrospinalfluid (CSF) and serum samples from patients with delirium. We hope to uncover new insights into the pathophysiology of delirium and explore its link to dementia.

NCT ID: NCT05055895 Recruiting - Alzheimer Disease Clinical Trials

Association of Anticholinergic Burden With Onset of Delirium in Older Adults With Alzheimer Dementia:

Start date: January 1, 2005
Phase:
Study type: Observational

Drugs with anticholinergic properties are commonly prescribed to older persons despite growing evidence of their significant adverse effects. However, limited data are available concerning their contribution to time of onset of delirium. This study aimed to determine the potential association of higher anticholinergic burden to early-onset of delirium superimposed dementia in the older adult.

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: NCT05029050 Recruiting - Delirium Clinical Trials

Dexmedetomidine or Clonidine Infusion for Prevention of Delirium After Open Heart Surgery

ALPHA2PREVENT
Start date: January 17, 2022
Phase: Phase 4
Study type: Interventional

A parallel-group treatment, five-centre, participant and investigator masked, three-arm study to assess the safety and effectiveness of dexmedetomidine or clonidine infusion compared to placebo for the prevention of delirium and cognitive decline in male and female participants aged 70+ scheduled for open heart surgery.

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