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Cognitive Dysfunction clinical trials

View clinical trials related to Cognitive Dysfunction.

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NCT ID: NCT02554253 Completed - Acute Kidney Injury Clinical Trials

The Impact of Ketamine on Postoperative Cognitive Dysfunction, Delirium, and Renal Dysfunction

Start date: September 2015
Phase: Phase 2
Study type: Interventional

Ketamine is a commonly used anesthetic medication which is used for induction of anesthesia as well as as an analgesic. It has been shown to have anti-inflammatory properties which may decrease post-operative complications following cardiac surgery with cardiopulmonary bypass that are thought to associated with inflammation. Some studies have shown that ketamine does decrease these complications when compared with anesthetics that are not commonly used in our cardiac anesthesiology practice. Propofol is another commonly used anesthetic medication which is used for induction of anesthesia. Ketamine has not been compared with propofol for potential to reduce post-operative complications associated with the inflammatory process. This study aims to see if ketamine will reduce the incidence of cognitive dysfunction, delirium, and renal dysfunction in comparison with propofol. In addition, the hemodynamic impact of ketamine compared propofol will be investigated.

NCT ID: NCT02553603 Completed - Clinical trials for Mild Cognitive Impairment

The Effect of Growth Hormone Releasing Hormone on Cognitive Function in Individuals With Mild Cognitive Impairment

Start date: July 18, 2017
Phase: Phase 1
Study type: Interventional

This study is examining the effects of growth hormone releasing hormone (GHRH) on mild cognitive impairment (MCI). GHRH will be given at a dose of 1mg/day for 10 weeks to subjects with MCI as well as healthy controls.

NCT ID: NCT02551952 Completed - Cognition Disorders Clinical Trials

Digital Game: A Scale to Evaluate the Perioperative Cognitive Function

MentalPlus®
Start date: July 8, 2021
Phase: N/A
Study type: Interventional

INTRODUCTION: Cognitive dysfunction is a frequent adverse event in the postoperative period, especially in elderly patients. The tests commonly used for the detection of postoperative cognitive dysfunction are time-consuming and with variable sensitivity and specificity and difficult routine use. Applying a difficult battery of cognitive tests decreases the viability of adopting measures to increase preoperative cognitive reserve and methods for prevention, diagnosis and rehabilitation of cases of Postoperative Cognitive Dysfunction (POCD), it is desirable to search for alternative methods diagnoses.

NCT ID: NCT02551419 Completed - Clinical trials for Mild Cognitive Impairment

Proof of Mechanism of a New Ketogenic Supplement Using Dual Tracer PET (Positron Emission Tomography)

BENEFIC
Start date: June 2015
Phase: N/A
Study type: Interventional

A six month, placebo-controlled, parallel group project in which MCI participants will receive 30 g/day of a custom-made MCT-based ketogenic supplement or a matching placebo. Uptake of both the brain's fuels - ketones (as 11C-AcAc) and glucose (as FDG) - both before and after the intervention will be assessed by PET (position emission tomography) ; imaging and ketone pharmacokinetic as primary objective as well as fMRI, diffusion MRI and cognition.

NCT ID: NCT02549560 Completed - Clinical trials for Postoperative Cognitive Dysfunction

Effects of the Transcranial Stimulation on Prevention of Cognitive Dysfunction in Cardiac Surgery

tDCS
Start date: July 8, 2021
Phase: N/A
Study type: Interventional

Postoperative cognitive dysfunction (POCD) is a contrary event observed between 20 to 83%, especially on elderly and patients submitted to cardiac surgery. The prevention and rehabilitation on cases of POCD can improve the quality of life and decrease the mortality in surgical patients. The effect of the noninvasive cerebral stimulation, also known as transcranial Direct Current Stimulation (tDCS) has been studied to be used in the treatment of brain injuries and depression, and also in the cognitive rehabilitation. The hypothesis is that the use of the tDCS technique can decrease the occurrence of POCD and cognitively rehabilitate patients submitted to cardiac surgeries.

NCT ID: NCT02544373 Completed - Multiple Sclerosis Clinical Trials

CPAP to Treat Cognitive Dysfunction in MS

Start date: November 12, 2015
Phase: N/A
Study type: Interventional

The objectives of this study are to determine the effects of obstructive sleep apnea (OSA) on cognitive function in patients with multiple sclerosis (MS); and to evaluate whether OSA treatment with positive airway pressure therapy could improve cognitive dysfunction in MS patients who have OSA.

NCT ID: NCT02536976 Completed - Parkinson Disease Clinical Trials

Mirabegron in Parkinson Disease and Impaired Cognition

MICT-PD
Start date: December 2015
Phase: Phase 4
Study type: Interventional

There is a high prevalence of OAB symptoms among patients with Parkinson's disease and a lack of pharmacotherapies with an acceptable side effect profile. Specifically, available anticholinergic medications have a high risk of cognitive side-effects, which preclude their use in PD patients with CI. PD can also cause a number of non-motor symptoms that are likely to be adversely affected by the currently available anticholinergic agents. Mirabegron is the first pharmacologic treatment which may not exacerbate CI, constipation, orthostatic hypotension (OH), somnolence, and dry mouth in PD.

NCT ID: NCT02536885 Completed - Clinical trials for Mild Cognitive Impairment

The Effect of Blood Pressure on the Postoperative Cognitive Dysfunction

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

Permanent and temporary cognitive impairment in the perioperative period is of great importance to patients. Hypoperfusion due to the intraoperative hypotension is often mentioned as a possible cause of postoperative cognitive dysfunction.

NCT ID: NCT02525198 Completed - Clinical trials for Mild Cognitive Impairment

The Cognitive Ageing Nutrition and Neurogenesis (CANN) Trial

CANN
Start date: August 1, 2015
Phase: N/A
Study type: Interventional

There is a dearth of research which takes a multi-compound approach to dietary interventions, in humans, aimed at improving outcome measures of cognition. Animal research in particular points towards fatty acids and flavonoids having a potentiating effect on each other, and possibly even being synergistic. Thus, study products will be administered in the present trial comprising both of these compounds, with a view to investigating their potential effects on cognition in older adults with mild cognitive impairment (MCI) or subjective memory impairment (SMI).

NCT ID: NCT02521818 Completed - Clinical trials for Mild Cognitive Impairment

Dietary Treatments for Cognitive Impairment in Older Adults

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

This trial seeks to establish the feasibility of implementing a ketogenic, modified Atkins diet (MAD) to older adults with mild cognitive impairment (MCI) or early Alzheimer's disease (AD) living in the community. A secondary aim is to determine whether adherence to the MAD results in better cognitive test scores than adherence to a non-ketogenic control diet. A final aim is to determine the role of apolipoprotein E (ApoE) genotype in participants' response to the MAD. Participants will be randomly assigned to a 12-week trial of either the MAD or a placebo diet based on the National Institute on Aging's recommendations for senior nutrition.