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Hypotension clinical trials

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NCT ID: NCT00846651 Completed - Hypotension Clinical Trials

Spinal Anesthesia Induced Hypotension During Cesarean Section

Start date: February 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare two methods for preventing low blood pressure associated with spinal anesthesia during Cesarean sections.

NCT ID: NCT00835224 Completed - Spinal Cord Injury Clinical Trials

Safety and Efficacy of L-NAME and Midodrine to Increase MAP

Start date: May 2010
Phase: Phase 2
Study type: Interventional

After a spinal cord injury the brain is no longer completely in control of the body below the level of injury. This affects many organs and systems in the body, we are interested in understanding how a spinal cord injury affects blood pressure and blood flow to the brain. We are going to study blood pressure while the person is seated in a wheelchair before and after we give the subject medications which should increase blood pressure in a laboratory setting and over the course of a normal day in persons with spinal cord injury.

NCT ID: NCT00824330 Completed - Diabetes Clinical Trials

Home-Based Walking Study in Older Adults With Type 2 Diabetes

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

Older persons with diabetes have a harder time maintaining blood pressure when standing up. When blood pressure drops when standing up, fainting may occur. This study will see how regular exercise can improve the ability of the body to keep blood pressure up when standing. We want to see how this improvement varies with a home-based walking program.

NCT ID: NCT00807976 Completed - Clinical trials for Diabetes Mellitus Type 2

Orthostatic Hypotension and Diabetes Mellitus

ODET
Start date: January 2009
Phase: N/A
Study type: Observational

Rationale: Orthostatic hypotension increases with age and is associated with increased vascular and all-cause mortality. The prevalence of orthostatic hypotension is also increased in diabetic subjects. In order to prevent related adverse events and vascular mortality it is of great interest to examine the prevalence of orthostatic hypotension in elderly diabetic subjects. Objective: To examine the prevalence of orthostatic hypotension and associated adverse events in type 2 diabetic elderly subjects. Study design: Cross-sectional observational study. Study population: Elderly type 2 diabetic subjects (70 years and older).

NCT ID: NCT00782340 Completed - Clinical trials for Dopamine Beta Hydroxylase Deficiency

A Clinical Study for Patients With Neurogenic Orthostatic Hypotension (NOH) Using Droxidopa

NOH301
Start date: September 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to see whether droxidopa is effective in treating symptoms of neurogenic orthostatic hypotension in patients with Primary Autonomic Failure (Pure Autonomic Failure, Multiple System Atrophy, Parkinson's Disease), Non-diabetic neuropathy, or Beta Hydroxylase deficiency.

NCT ID: NCT00781157 Completed - Hypotension Clinical Trials

Phenylephrine for Spinal Induced Hypotension

Start date: January 2008
Phase: Phase 4
Study type: Interventional

This study is designed to determine the ED90 for a single dose of phenylephrine for the treatment of spinal induced hypotension in parturients presenting for an elective CD. The ED90 is the effective dose at which 90% of subjects will have a "positive" response to phenylephrine. The primary outcome measure is the ED90 for bolus phenylephrine. Secondary outcomes include the need for additional vasopressors, glycopyrolate to treat bradycardia, and the presence of hypertension following administration of phenylephrine.

NCT ID: NCT00777166 Completed - Myocardial Ischemia Clinical Trials

Cardiac Effects of Oxytocin Administrated During Cesarean Section, Signs of Myocardial Ischemia

Start date: December 2005
Phase: Phase 4
Study type: Interventional

Oxytocin has cardio vascular effects as hypotension, tachycardia and possibly coronary spasm. The uterotonic effect of the drug is used during cesarean section, to minimize blood loss.ECG changes suggestive of cardiac ischemia (ST depression) has been showed in previous studies of patients undergoing cesarean section i regional anaesthesia. The effect of oxytocin on this outcome has not been investigated to any extent. In the current study, we tested the hypothesis that there was no difference in occurrence of ECG changes (ST segment depression) between two doses of oxytocin. Participants were randomized to receive either 5 or 10 units of oxytocin in a double blinded fashion. Main outcome measure is occurrence of significant ST depression on ECG. Secondary outcome measures are mean arterial pressure, heart rate, blood loss, symptoms as chest pain, shortness of breath and feeling of heaviness on the chest.

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: NCT00738062 Completed - Clinical trials for Multiple System Atrophy

Open-Label Clinical Study of Droxidopa in Patients With Neurogenic Orthostatic Hypotension (NOH)

NOH303
Start date: January 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the durability of effect of Droxidopa in treating symptoms of neurogenic orthostatic hypotension in patients with Primary Autonomic Failure (Pure Autonomic Failure, Multiple System Atrophy, Parkinson's Disease), Non-diabetic neuropathy, or Beta Hydroxylase deficiency.

NCT ID: NCT00721604 Completed - Hypotension Clinical Trials

Fluid Responsiveness Prediction at the Bedside

Start date: July 2008
Phase: N/A
Study type: Observational

The purpose of this study is to verify the accuracy and applicability of predictors of fluid administration efficacy in hypotensive critically ill patients.