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Primary Dysautonomias clinical trials

View clinical trials related to Primary Dysautonomias.

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NCT ID: NCT00878033 Completed - Clinical trials for Chronic Renal Failure

Autonomic Dysfunction and Inflammation in Chronic Hemodialysis Patients

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

This study investigates the relationship between autonomic dysfunction and chronic inflammation in hemodialysis patients.

NCT ID: NCT00844935 Withdrawn - Clinical trials for Cardiovascular Abnormalities

Electrocardiographic Autonomic Function Measures in Mechanically Ventilated Patients

Start date: September 2011
Phase: N/A
Study type: Observational

This research proposal has two main objectives. The first is to increase understanding of the underlying physiological interactions that occur between the cardiovascular, pulmonary, and ANS during transition between positive pressure mechanical ventilation (MV) and spontaneous breathing. The second is to determine if heart rate variability, (HRV) a reflection of autonomic nervous system (ANS) activity, and autonomic information flow (AIF), a set of nonlinear measures derived from HRV, both measured in the intensive care unit (ICU) can predict patient outcomes including successful weaning and in-hospital recovery time after an episode of cardiopulmonary compromise requiring MV. Hypothesis 1. Transitions between mechanically supported ventilation and spontaneous breathing will disturb cardiovascular synchrony, altering the relationship of HRV, AIF, respiratory rate, and blood pressure; Hypothesis 2. More normal HRV and AIF values, measured during baseline MV and sedation awakening (a period immediately prior to SBT when sedative medications are discontinued) will be associated with easier weaning, and shorter intensive care unit (ICU) and hospital lengths of stay; more abnormal measurements will be associated with longer lengths of stay; Hypothesis 3. AIF is a more sensitive predictor of successful weaning from MV than HRV.

NCT ID: NCT00780650 Completed - Type 1 Diabetes Clinical Trials

Mechanisms of Hypoglycemia Associated Autonomic Dysfunction, Q4-Atomoxetine

Start date: May 2009
Phase: Early Phase 1
Study type: Interventional

This study is aimed at determining if the drug Atomoxetine (Strattera-used to treat Attention Deficit Hyperactivity Disorder(ADHD) has effects on the body's ability to defend itself against low blood sugar.

NCT ID: NCT00780390 Terminated - Clinical trials for Complex Regional Pain Syndrome

Autonomic Dysfunction and Spinal Cord Stimulation in Complex Regional Pain Syndrome

CRPS
Start date: January 2008
Phase: N/A
Study type: Interventional

To demonstrate that spinal cord stimulator has an effect on sympathetic function (the one that give us the fight and flight response). Therefore, if the spinal cord stimulator has an effect on sympathetic function, the responses from CRPS patients to different stimuli will differ significantly pre and post SCS implant. If CRPS patients exhibit autonomic, CRPS patients could be stratified according to their sympathetic function pre-implant. It is expected that patients with a moderate/mild form of autonomic dysfunction will have better outcomes with the SCS.

NCT ID: NCT00775853 Completed - Parkinson Disease Clinical Trials

Biomarkers of Risk of Parkinson Disease

Start date: May 27, 2009
Phase:
Study type: Observational

This study (https://pdrisk.ninds.nih.gov) will determine if people who have risk factors for Parkinson disease (PD) have biomarkers (objective ways to measure a disease process) that show that the disease process is actually going on, and if people who have abnormal biomarkers go on to develop PD during several years of follow-up. Biomarkers of Parkinson disease (PD) might identify people who are healthy now but may develop the disease later in life. Healthy volunteers and people who have certain risk factors for developing PD who are between 18 and 70 years of age may be eligible for this study. People with the following risk factors are included: - Family history of PD - Loss of sense of smell - Fall in blood pressure when standing up - REM behavior disorder (a type of sleep disturbance) Participants undergo the following tests and procedures: - Screening examination - Medical and neurological history and physical examination - Tests or rating scales for movement, sense of smell, mood, attention, fatigue, pain, and thinking. - Measurement of blood pressure and pulse rate while lying down and then standing up - Blood draw for genetic testing - Inpatient testing at the NIH Clinical Center for 2-3 days, including: - Measurements while blowing against a resistance - Measurements of blood pressure and pulse rate - Blood draws for levels of various chemicals - PET and MRI scanning - Lumbar puncture (spinal tap) - Electrocardiogram - Skin electrical conduction test (test of sweat production) - Skin and core temperature measurements - Transcranial ultrasound (sound-wave test of the head) - Follow-up testing (up to five visits in 18-month intervals) to repeat some of the tests listed above, excluding the genetic testing and spinal tap

NCT ID: NCT00748059 Completed - Clinical trials for Orthostatic Hypotension

The Pathophysiology of Orthostatic Hypotension

Start date: December 1996
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the cause of low blood pressure in selective patients who have problems with their involuntary (autonomic) nervous system. These patients frequently have had symptoms throughout their life, and their disorder might have a genetic basis. The biochemical, physiological and pharmacological procedures in this study should help us define the problem and perhaps lead to more effective treatment.

NCT ID: NCT00742521 Completed - Type 1 Diabetes Clinical Trials

Mechanisms of Hypoglycemia Associated Autonomic Dysfunction, Q.3

Start date: March 2001
Phase: N/A
Study type: Interventional

It has been found that in some cases, when a person with Diabetes Mellitus has an episode of low blood sugar,or hypoglycemia, and then later exercises, he or she is vulnerable to another bout of hypoglycemia during that exercise. The purpose of this study is to determine what factors during the previous bout of hypoglycemia might cause another bout of hypoglycemia while exercising later.

NCT ID: NCT00715065 Withdrawn - Syncope Clinical Trials

fMRI in Blood Phobia Syncope

Start date: June 2010
Phase: N/A
Study type: Observational

We plan to study patient who faint in response to the sight of blood and compare them to healthy subjects who do not. We are going to use a special type of MRI scan (functional MRI) to determine if there are differences in brain activation in response to seeing bloody or gory pictures that occur before the fainting occurs.

NCT ID: NCT00581477 Terminated - Clinical trials for Orthostatic Hypotension

Treatment of Orthostatic Hypotension

Start date: January 2004
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to try different medications in patients with low blood pressure and other problems with their involuntary (autonomic) nervous system. The pharmacological trials in this study will perhaps lead to more effective treatment. The protocol includes single dose trials, dose-selection trials, 5-day trials and chronic (approximately 2 months) trials, although only dose-selection trials were consistently performed and have results presented.

NCT ID: NCT00574639 Completed - Type 1 Diabetes Clinical Trials

Mechanisms of Hypoglycemia Associated Autonomic Dysfunction Question 2

Alp Ex
Start date: July 2007
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to determine the way by which Alprazolam (Xanax) an anti-anxiety drug affects specialized molecules in your brain called GABA (A) receptors that alter your body's ability to defend itself from low blood sugar (hypoglycemia). We hypothesize that prior activation of GABA (A) receptors may result in blunting of counterregulatory responses during subsequent hypoglycemia and exercise.