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Unconsciousness clinical trials

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NCT ID: NCT01787903 Completed - Clinical trials for Type 1 Diabetes Mellitus

The Effects of RT-CGM on Glycemia and QoL in Patients With T1DM and IHA

INCONTROL
Start date: February 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine what the effects are of real-time continuous glucose monitoring on glycemia and quality of life in patients with type 1 diabetes mellitus and impaired hypoglycemia awareness.

NCT ID: NCT01778608 Completed - Conscious Sedation Clinical Trials

Feasability Test of a Handset Device to Detect Levels of Sedation and Loss of Consciousness

Start date: January 2012
Phase:
Study type: Observational

Sedation is often administered to relieve anxiety and discomfort during uncomfortable procedures in elderly patients. Patient control of sedation offers many potential benefits for patients and healthcare professionals, including improved safety and patient satisfaction. The investigators overall goal is to develop a patient controlled intravenous sedation system that is effective but very safe for the patient, and requires minimal supervision by a doctor or nurse. To fulfill these criteria, a sedation system should incorporate fail-safe safety mechanisms. A key safety-critical component is a method of objectively assessing the degree of sedation of the patient, and of preventing him from self-administering unsafe doses of the sedative drug. The investigators have designed a new sedation system that uses a measure of the speed of response of the patient to a defined non-noxious stimulus to determine whether or not it is safe to allow him to self-administer further levels of sedation. Before being able to execute a volunteer study in order to determine a rational selection of optimal threshold response time, a feasibility test on the handset device is required.

NCT ID: NCT01768416 Completed - Clinical trials for Loss of Consciousness at End of Life

Measuring Depth of Unconsciousness at the End of Life Using Bispectral Index (BIS)

BISSOPS
Start date: March 1, 2013
Phase:
Study type: Observational

The purpose of this study is to use the BIS monitor to assess the degree of consciousness in pre-terminal palliative patients admitted to our palliative care unit and to ascertain if this tool provides a more accurate assessment of consciousness in this specific group of patients than clinical observation of consciousness and the use of sedation scales. We hypothesize that the measured BIS results provide a more accurate assessment of the patient's level of consciousness than routine clinical observation or the use of sedation scales.

NCT ID: NCT01721369 Completed - Clinical trials for Brief Loss of Consciousness

Applicability of Syncope Guidelines in Cataluña

SYNCAT
Start date: November 2011
Phase:
Study type: Observational

The aim of SYNCAT study is to study the level of adherence of the centers in Cataluña tu the Syncope Guidelines ESC2009 for the diagnosis and treatment of syncope and the impact that following them can have in the prognosis of these patients.

NCT ID: NCT01611194 Completed - Clinical trials for Post-Concussion Syndrome

mTBI Mechanisms of Action of HBO2 for Persistent Post-Concussive Symptoms

BIMA
Start date: September 11, 2012
Phase: Phase 2
Study type: Interventional

Purpose of this study is to investigate the mechanisms of action of hyperbaric oxygen therapy for persistent post-concussive symptoms after mild tramatic brain injury

NCT ID: NCT01474889 Completed - Healthy Clinical Trials

Glucose Counterregulation in Long Standing Type 1 Diabetes

Start date: October 2011
Phase: N/A
Study type: Interventional

Enrollment for this study is complete. This study is designed to determine if use of a real-time continuous glucose monitor (RT-CGM) can reverse defective Glucose counter regulation and hypoglycemia unawareness in long standing type 1 diabetes.

NCT ID: NCT01339806 Completed - Clinical trials for Traumatic Brain Injury With Brief Loss of Consciousness

The Study of Cognitive Rehabilitation Effectiveness for Mild Traumatic Brain Injury

SCORE
Start date: June 2011
Phase: Phase 4
Study type: Interventional

The objective of this trial is to evaluate the effectiveness of cognitive rehabilitation in OIF/OEF service members with a history of mild traumatic brain injury and persistent (3-24 months post injury) cognitive complaints. This is a prospective, randomized, control treatment trial of cognitive rehabilitation for OEF/OIF Service Members with a history of mild traumatic brain injury (mTBI) and persistent (3-24 months post-injury) cognitive complaints. Subjects will be recruited from consecutive patient referrals to the TBI Service at SAMMC-North. Patients who meet eligibility criteria and consent to participate in the treatment trial will be randomly assigned to one of four, 6-week treatment arms of the study. Subjects will be evaluated prior to the start of treatment and 3, 6, 12, and 18 weeks following the initiation of the study. The total number of patients to be studied is 160 (maximum), which is approximately 20 patients per month.

NCT ID: NCT01315171 Completed - Clinical trials for Type 1 Diabetes Mellitus

Effect of a Medium Chain Triglyceride Supplemented Diet on Cognitive Function and Brain Activation in Type 1 Diabetes.

Start date: January 2012
Phase: N/A
Study type: Interventional

Insulin treatment often causes the blood glucose levels to fall too low (hypoglycemia). Hypoglycemia can be associated with confusion and disorientation as well as other symptoms such as palpitations, sweating and tremors. Medium chain triglycerides (MCT) can be used as a fuel in the brain during low blood sugar levels and therefore may prevent or reduce some of the confusion and disorientation seen during hypoglycemia. We would like to determine if a diet supplemented with medium chain triglycerides can improve cognitive function during hypoglycemia, diabetes control and also look at brain activity.

NCT ID: NCT01091350 Completed - General Anesthesia Clinical Trials

Influence of Equilibration Rate Constant (ke0) of Propofol on the Effect Site Concentration for Loss of Consciousness

Start date: May 2009
Phase: N/A
Study type: Interventional

The aim of this study is to validate that an effect compartment concentration for loss of consciousness (LOC) was varied according to different Keo value.

NCT ID: NCT01053078 Completed - Type 1 Diabetes Clinical Trials

Naltrexone and Hypoglycemia in Type 1 Diabetes

Naltrexone
Start date: October 2009
Phase: Phase 1/Phase 2
Study type: Interventional

Low blood sugar is also called hypoglycemia. Usually, it is mild and can be treated quickly and easily by eating or drinking a small amount of a sugar-rich food. If low blood sugar is left untreated, it can get worse and cause confusion, clumsiness or fainting. Severe hypoglycemia can lead to seizures, coma, and even death. Some people with diabetes do not have early warning signs of low blood sugar. This condition is called hypoglycemia unawareness. It happens when the body stops reacting to low blood sugar levels and the person does not realize that they need to treat their hypoglycemia. This can lead to more severe and dangerous hypoglycemia. The purpose of this early study is to see if a drug called naltrexone should be studied more in people with Type I diabetes and hypoglycemia unawareness. This study will show whether naltrexone could reduce hypoglycemia unawareness. The study will also show, by using magnetic resonance imaging (also called MRI), whether naltrexone changes the way blood flows in the brain when a person is experiencing hypoglycemia.