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Unconsciousness clinical trials

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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NCT ID: NCT01498471 Withdrawn - Syncope Clinical Trials

NICE Guideline 'Red Flags' to Predict Serious Outcome After Transient Loss of Consciousness

Start date: January 2012
Phase:
Study type: Observational

This study is designed to evaluate the accuracy of the National Institute for Health and Clinical Excellence (NICE) guideline 'red flags' to identify patients at high risk of short term serious outcome when presenting in the emergency department (ED) with Transient Loss of Consciousness (TLoC). Red flags were defined as ECG abnormality, history or physical signs of heart failure, TLoC during exercise, family history of sudden cardiac death at an age < 40 years and/or an inherited cardiac condition, new or unexplained breathlessness, heart murmur, absence of prodromal symptoms in any patient aged > 65 years.

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.

NCT ID: NCT01029639 Withdrawn - Hypoglycemia Clinical Trials

Effects of Pulsatile Intravenous Insulin Delivery on Hypoglycemic Unawareness

Start date: January 2007
Phase: Phase 2/Phase 3
Study type: Interventional

Hypoglycemic unawareness is a major problem in the treatment of Diabetes Mellitus. Hypoglycemic unawareness is the inability to recognize or sense early symptoms of low blood sugar. This study was instituted to evaluate the effect of Pulsatile intravenous (IV) Insulin on improving or reinstating the diabetics ability to sense or feel the symptoms associated with low blood sugar.

NCT ID: NCT01011192 Completed - Unconsciousness Clinical Trials

Performance of Two Different ke0s in the Same Pharmacokinetic Propofol Model

Start date: September 2009
Phase: N/A
Study type: Observational

The aim of this study was to assess the clinical performance of two different ke0s (fast and slow) in terms of propofol effect-site concentration (Ce) during the loss and recovery of consciousness, using Marsh's pharmacokinetic model.The hypothesis to be tested was that the Ce of propofol predicted by the slow ke0 in the loss and recovery of consciousness is similar, differently from the fast ke0.

NCT ID: NCT00869154 Completed - Clinical trials for Traumatic Brain Injury With Brief Loss of Consciousness

Multidisciplinary Treatment in Patients With Mild Traumatic Brain Injury

Start date: March 1, 2009
Phase: N/A
Study type: Interventional

The aim of the study is to compare a multidisciplinary examination and follow up by rehabilitation program with a multidisciplinary examination, good advice and follow up by the family doctor. Further on we will examine if there were differing clinical characteristics between patients who attended a planned follow-up session and those that failed to and Prognostic factors in mild traumatic brain injury patients after discharge from hospital.