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Orthostatic Intolerance clinical trials

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NCT ID: NCT00581022 Completed - Clinical trials for Postural Tachycardia Syndrome

Objective Sleep Disturbances in Orthostatic Intolerance

Start date: November 2006
Phase:
Study type: Observational

We wish to study sleep architecture in patients with chronic orthostatic intolerance. We will test the null hypothesis that there is no difference in time during the various phases of sleep between patients and healthy control subjects.

NCT ID: NCT00580619 Completed - Clinical trials for Chronic Fatigue Syndrome

Autonomic Nervous System and Chronic Fatigue Syndrome

CFS&ANS
Start date: April 2007
Phase: Phase 1
Study type: Interventional

The investigators propose to test the hypothesis that the sympathetic nervous system contributes to the cardiovascular and inflammatory abnormalities present in the chronic fatigue syndrome (CFS) and, in particular in the subset of patients characterized by postural tachycardia syndrome (POTS). CFS and POTS are seen mostly in otherwise normal young women, and are the cause of significant disability. A substantial proportion of patients referred for evaluation of POTS met diagnostic criteria for CFS and, conversely, a subset of patients referred for treatment for CFS have POTS. The investigators hypothesize that sympathetic activation underlies the pathophysiology of patients in whom CFS and POTS overlap (CFS-P).

NCT ID: NCT00262470 Active, not recruiting - Tachycardia Clinical Trials

Treatment of Orthostatic Intolerance

Start date: April 1997
Phase: Phase 1/Phase 2
Study type: Interventional

This trial is designed to study the effects of various mechanistically unique medications in controlling excessive increases in heart rate with standing and in improving the symptoms of orthostatic intolerance in patients with this disorder.

NCT ID: NCT00175773 Completed - Spinal Cord Injury Clinical Trials

Mechanisms of Orthostatic Intolerance in Spinal Cord Injured Individuals and Following Bed Rest

Start date: November 2004
Phase:
Study type: Observational

The primary purpose of this study is to investigate the relationship between the extent of neurologic (nerve) impairment in patients with spinal cord injuries and how well the nerves passing down the spine to the heart and blood vessels are working. These nerves are called the descending spinal sympathetic pathway (DSSP) and are important in controlling many functions, including blood pressure. We also wish to examine how injury severity and DSSP function influence blood levels of nor-epinephrine and epinephrine. Nor-epinephrine and epinephrine are hormones released into the blood that are also important in controlling blood pressure. Thus, we will also look at how the effect of the extent of DSSP dysfunction influences heart rate and blood pressure and blood levels of certain enzymes.

NCT ID: NCT00069693 Completed - Syncope Clinical Trials

Evaluation of Chronic Orthostatic Intolerance

Start date: September 26, 2003
Phase: N/A
Study type: Observational

This study will conduct tests with patients with primary chronic orthostatic intolerance (COI) to learn more about this disorder of the autonomic nervous system. Healthy normal volunteers and patients 18 years of age and older with COI may be eligible for this study. Participants undergo one or more of the following tests and procedures: - Blood studies, including arterial catheter insertion to measure blood pressure and collect arterial blood samples, blood flow studies using sensors applied to the skin and a pressure cuff around a limb, blood volume studies using injection of radioactively labeled human serum albumin and gene studies to look for genetic abnormalities associated with certain proteins. - Imaging studies, including CT scan of the adrenal glands, heart ultrasound, and PET scanning. - Electrocardiogram - Microdialysis to measures levels of chemicals in the body fluid of certain tissues. A thin tube is inserted into the skin and a solution is passed through it. Chemicals in the body tissues enter the solution in the tube. The solution is collected and the chemical levels are measured. - Neck suction. Neck suction is applied to test a reflex the brain uses to regulate blood pressure. - Perometry. Limb volume is measured using an infrared light that moves up the limb. - Quantitative sudomotor axon reflex test to evaluate an aspect of autonomic nervous system function. A small amount of a brain chemical (acetylcholine) is applied to the skin with a tiny amount of electricity, and the sweat in a nearby patch of skin is measured. - Skin electrical conduction test using sensors on the skin to measure sweat production. - Skin and core temperature measurements using sensors on the skin and in the ear canal. - Tilt table test. The subject lies on a table, secured with straps around the chest and legs. Sensors are placed on the arms and chest to monitor blood pressure, pulse rate, and heart rhythm. A catheter is placed in a vein in each arm to collect blood samples and give drugs. Another catheter is placed in an artery to draw blood and monitor blood pressure. The subject is given an infusion of norepinephrine and epinephrine, and baseline measures and blood samples are taken. The table is tilted upright and more measurements and blood samples are taken at intervals for up to 30 minutes. The table is returned to a horizontal position and additional measurements and samples may be taken. Drugs may be administered during the tests, including acetylcholine, epinephrine, and norepinephrine, radioactive chemicals used in imaging studies, and drugs that affect blood vessels, heart rate, and force of heart contractions.