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Delirium clinical trials

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NCT ID: NCT03218358 Recruiting - Delirium Clinical Trials

Effect of the Intra-abdominal Pressure on the Risk of Delirium in Mechanically Ventilated Patients.

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

intra-abdominal hypertension (IAH) and delirium are serious, high-frequency complications in intensive care unit (ICU) patients. The consequences of the complication range from high morbidity and mortality to a greater need for nursing care. We hypothesize that there could be a correlation between IAH and incidence of delirium.

NCT ID: NCT03215745 Recruiting - Clinical trials for Hyperactive Delirium

Delirium Prevention in Patients From the Intensive Care Unit (DELA)

DELA
Start date: October 1, 2017
Phase: N/A
Study type: Interventional

"To determine the efficacy of program of prevention of delirium in critically ill patients from the intensive care units of Bucaramanga and Floridablanca. Methods: The study will be a randomized controlled clinical trial in 600 critically ill patients recruited at 24 hours from arrival on the intensive care units of Bucaramanga and Floridablanca, without delirium, with ≥50% in the PREDELIRIC scale score, who comply with the inclusion and exclusion. The patients will be randomized in blocks to one of the two groups, intervention group (delirium prevention program, n=200) with control group (usual care; n= 400), the study will compare the incidence of delirium in both groups. Patients will be followed every day with Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) until the patient presents delirium, exit to hospitalization or death. Delirium prevention program includes individualized nonpharmacological interventions such as multisensory stimulation, cognitive stimulation, activate the functional and family involvement. The study has received ethical approval from the University of Santander"

NCT ID: NCT03199950 Recruiting - Delirium Clinical Trials

PROfylactic Haloperidol in Patients Defined as High Risk for DElirium With Delirium Risk mOdel

PRODEO
Start date: June 23, 2017
Phase: Phase 4
Study type: Interventional

The hospital pharmacy at the Zuyderland Medical Centre developed the DElirium MOdel (DEMO) to predict which patients are at risk of developing a delirium in patients aged 60 or older. With this delirium risk prediction model we aim to predict more accurately which patients are at high risk of developing a delirium and want to investigate if these patients can benefit from prophylactic haloperidol.

NCT ID: NCT03171766 Recruiting - Clinical trials for Postoperative Complications

Pre-operative Neurocognitive Disorder and Low Near-infrared Spectrometry is Associated With Postoperative Delirium

Start date: June 15, 2017
Phase: N/A
Study type: Observational

The main goal of the investigation is to identify the incidence of cognitive dysfunction and POD in patients older than 65 years of age undergoing neurosurgical elective surgery and determine if an association between cognitive dysfunction, basal NIRS and POD exists.

NCT ID: NCT03165539 Recruiting - Delirium Clinical Trials

Cerebral Oxygen Desaturation and Post-Operative Delirium in Thoracic Surgical Patients

Start date: September 2015
Phase:
Study type: Observational

This study will assess the incidence and risk factors for post-operative delirium in patients undergoing thoracotomy. Specifically, the study will assess if there is any relationship between an intra-operative decrease in brain oxygen levels which can occur during one-lung ventilation, and the occurrence of delirium in the post-operative period.

NCT ID: NCT03158909 Recruiting - Delirium Clinical Trials

Trial of a Non-pharmacological Intervention to Prevent Delirium Among Elderly In-patients

Start date: January 15, 2020
Phase: N/A
Study type: Interventional

This study evaluates the effect of earplugs and eyemask for delirium prevention among elderly in-patients. Half of patients will receive earplugs and eyemask for use during the night and information about orientation to time and space every night, while the other half will receive only the time and space orientations.

NCT ID: NCT03149783 Recruiting - Pain, Postoperative Clinical Trials

Study to Determine if Pre- and Post- Operative TAP Catheters With Ropivacaine Versus Placebo Affects Anesthetic, Narcotic Dosing, and Pain Scores

TAP RCT
Start date: February 13, 2018
Phase: Phase 2
Study type: Interventional

A randomized controlled trial to determine if pre- and post- operative regional pain control (transversus abdominis plane block) with ropivacaine versus placebo leads to lower anesthetic and narcotic dosing, and alters pain scores. This study plans to learn more about regional anesthesia and pain control during abdominal surgery. The study will gather data about the effectiveness of continuous catheter infusion of local anesthetic after an abdominal operation. Outcomes include pain scores, IV pain medicine requirements, and delirium.

NCT ID: NCT03141619 Recruiting - Critical Illness Clinical Trials

Cerebral Oxygenation and Neurological Outcomes FOllowing CriticAL Illness-2

CONFOCAL-2
Start date: October 13, 2017
Phase:
Study type: Observational

This study is designed to test the hypothesis that poor cerebral perfusion during critical illness is a risk factor for acute and long-term neurological dysfunction among survivors. We use near-infrared spectroscopy to measure brain tissue oxygenation as a non-invasive surrogate marker for cerebral perfusion. Acute neurological dysfunction is defined as the presence of delirium, which is assessed using the Confusion Assessment Method-Intensive Care Unit (CAM-ICU). Chronic neurological dysfunction is defined as having quantitative impairments on robotic testing (KINARM robot) and traditional neuropsychological screening (Repeatable Battery for the Assessment of Neuropsychological Status).

NCT ID: NCT03124303 Recruiting - Delirium Clinical Trials

Interventions for Postoperative Delirium: Biomarker-3

IPOD-B3
Start date: February 13, 2017
Phase:
Study type: Observational

The IPOD-B3 study aims to characterize the relationship between premorbid brain activity and postoperative delirium in patients undergoing major surgery. This is a expansion of the NeuroVISION Bolt-On study, NCT01980511.

NCT ID: NCT03013790 Recruiting - Delirium Clinical Trials

Melatonin Use in the Intensive Care Elderly Population

MICE
Start date: December 2016
Phase: Phase 4
Study type: Interventional

The investigators are studying the use of Melatonin in non-ventilated patients over the age of 65. Primary endpoint will be assesments of delirium, with secondary endpoints to include length of stay, use of anti-psychotic medications, and mortality