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Cognition Disorders clinical trials

View clinical trials related to Cognition Disorders.

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NCT ID: NCT02656901 Completed - Clinical trials for Postoperative Cognitive Dysfunction

Early Postoperative Cognitive Dysfunction After Closed Loop Anesthesia vs Inhalational Anesthesia or TIVA

Start date: January 2016
Phase: N/A
Study type: Interventional

This study is designed to test the hypothesis that closed loop system reduces post operative cognitive dysfunction incidence 15 min after anesthesia more than desflurane, sevorane, total intravenous anesthesia manually guided by bispectral index in urologic surgical patients. The secondary aim is to evaluate the postoperative cognitive impairment in in elderly vs younger surgical patients.

NCT ID: NCT02591316 Completed - Breast Cancer Clinical Trials

Nutrition, Physical Activity, and Cognition in Breast Cancer Survivors

Start date: February 2015
Phase: N/A
Study type: Observational

The purpose of this study is to examine the relationship between nutrition, physical activity and brain function in breast cancer survivors.

NCT ID: NCT02575482 Completed - Cognitive Disorders Clinical Trials

A Study to Investigate the Safety, Tolerability and Pharmacokinetics of SUVN-D4010 in Healthy Subjects

Start date: July 2015
Phase: Phase 1
Study type: Interventional

The purpose of this study is to investigate the safety, tolerability and pharmacokinetics of SUVN-D4010 in healthy male subjects following single or multiple ascending doses.

NCT ID: NCT02574234 Completed - Delirium Clinical Trials

Influence of Apelin Levels on Postoperative Cognitive Disorders After Orthopedic Surgery in Elderlies (APOCOGNIT)

APOCOGNIT
Start date: March 30, 2016
Phase: N/A
Study type: Interventional

No successful strategy is proposed to patients submitted to important surgery to reduce the incidence of postoperative cognitive disorders (POCD) onset. This project propose to measure plasma levels of apelin in wide population submitted to orthopedic surgery. Apelin could be involved in anti-inflammatory processes. Apelin levels before and after surgery correlated to postoperative cognitive disorders symptom measured by PET-Scan could be an important predictive or diagnostic marker to adapt therapeutic strategy to fight against postoperative cognitive disorders.

NCT ID: NCT02572219 Completed - Hypertension Clinical Trials

Effects of a Nutraceutical Preparation on Cognitive Impairment in Hypertensive Patients

Start date: November 2015
Phase: Phase 3
Study type: Interventional

Aim of this randomized, double-blind clinical study is to evaluate the efficacy of a nutraceutical preparation on early markers of cognitive impairment, in patients affected by arterial hypertension.

NCT ID: NCT02571504 Completed - Clinical trials for Cognitive Impairment

Cognitive Training for the Remediation of Functional Brain Health in HIV

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

Cognitive deficits in HIV reflect degraded brain network functioning that may be amenable to remediation through cognitive training. In this sub-study, we will make use of Plasticity-based Adaptive Cognitive Remediation (PACR), which applies well-understood techniques derived from brain plasticity and implicit/procedural/perceptual learning to improve the speed and accuracy of information processing, with exercises that are designed to drive generalized improvements. Simultaneously, these exercises heavily engage neuromodulatory systems to re-establish their normal control over learning and memory. As an individual restores these degraded abilities through intensive procedural learning, the encoding of naturalistic information significantly improves, and all resulting declarative memory and cognitive functions based on the quality of that incoming information necessarily improve as well, leading to improvement that generalizes beyond the trained tasks. A subset of 80 HIV+ individuals will undergo eight weeks of PACR to determine its feasibility and appropriateness for people with mild cognitive difficulties related to HIV infection. The results of this study are expected to be pivotal in generating data to create an optimal training program aimed at stabilizing or improving brain function in HIV infected individuals experiencing cognitive decline.

NCT ID: NCT02570997 Completed - Clinical trials for Cognitive Impairment

Ascending Dose Study of CT1812 in Healthy Volunteers

Start date: September 2015
Phase: Phase 1
Study type: Interventional

This is a double-blind, placebo controlled, ascending dose, multi-cohort trial. The study will be conducted in two phases: a single ascending dose (SAD) phase "Part A", followed by a multiple ascending dose (MAD) phase "Part B". In Part A, subjects will receive one dose of study drug. In Part B, subjects within a cohort will receive the same dose daily for 14 days. In both parts, sequential cohorts will be exposed to increasing doses of CT1812 in order to identify the maximum tolerated dose (MTD).

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: NCT02552329 Completed - Clinical trials for Mild Cognitive Impairment

Effects of Tai Chi Exercise on Cognition and Serum Biomarkers of Individuals With MCI

MCI-TaiChi
Start date: December 2013
Phase: N/A
Study type: Interventional

Most research on Tai Chi has been done in the area of balance and falls. Studies examining the effects of Tai Chi exercise on cognitive function are sparse especially in the population of MCI. Therefore, the aims of the present study are: 1) to examine the effects of Tai Chi exercise on cognitive function of elderly with MCI, and 2) to investigate the effects of 6-month Tai Chi exercise on serum biomarkers in individuals with MCI.

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.