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Hypotension clinical trials

View clinical trials related to Hypotension.

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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.

NCT ID: NCT00694343 Completed - Hypotension Clinical Trials

Efficacy of Voluven® for the Prevention of Hypotension During Spinal Anesthesia for Cesarean Section

CAESAR
Start date: June 2008
Phase: Phase 4
Study type: Interventional

The aim of the study is to evaluate the efficacy of Voluven® in the prevention of maternal hypotension in women undergoing spinal anesthesia for cesarean section

NCT ID: NCT00664079 Terminated - Respiratory Failure Clinical Trials

Thyroid Hormones in Critically Ill Children

Thyroid
Start date: October 2005
Phase: N/A
Study type: Observational

Thyroid hormones are substances naturally made by the body and are important to many of your body's basic functions such as breathing and brain function. We are investigating whether or not these hormones are at lower levels in critically ill children which could lead to further health problems. We hope to get a better understanding of hormone levels and their effects on critically ill children to better help other children in the future.

NCT ID: NCT00657046 Completed - Clinical trials for Intradialytic Hypotension

Safety and Benefit Study of Droxidopa to Treat Patients With Intradialytic Hypotension

IDH201
Start date: December 2007
Phase: Phase 2
Study type: Interventional

In clinical trials in Japan, droxidopa has been shown to be effective in affecting blood pressure changes upon orthostatic challenge in patients with autonomic dysfunction, as well as reducing the severity and frequency of symptoms of orthostatic hypotension in these patients. The efficacy of droxidopa in ameliorating symptoms in patients undergoing dialysis has also been demonstrated in the literature and clinical trials conducted in Japan. The current study will investigate the clinical efficacy of two different doses of droxidopa in patients with intradialytic hypotension over a 4 week treatment period with a placebo control. The clinical efficacy will be evaluated by changes in hypotension- related symptoms, as well as changes in blood pressure prior to, during and following, HD sessions as compared to their pre-treatment baseline values.

NCT ID: NCT00654693 Completed - Hypertension Clinical Trials

NTX Wireless Patient Monitoring System

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

- Determine the accuracy of the NTX wireless monitoring system alerts - Evaluate patient compliance with wearing device - Determine false alarm rates

NCT ID: NCT00644644 Completed - Hypertension Clinical Trials

Validation of the NTX Wireless Patient Monitoring System

TATRC
Start date: March 2008
Phase: N/A
Study type: Observational

- Reduction in time to detection of Clinically Significant events - Reduction of time to Intervention during Clinically Significant events - Reduction in the number of admissions to Intensive Care

NCT ID: NCT00633880 Completed - Clinical trials for Dopamine Beta Hydroxylase Deficiency

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

NOH302
Start date: January 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: 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: NCT00581373 Active, not recruiting - Clinical trials for Orthostatic Hypotension

Water and the Gastropressor Response - Diurnal Variability

Start date: August 2007
Phase: N/A
Study type: Interventional

We will test the null hypothesis that there is no diurnal (morning to afternoon)variability in the blood pressure response to the ingestion of water 16 oz.

NCT ID: NCT00580996 Active, not recruiting - Clinical trials for Orthostatic Hypotension

Water and the Gastropressor Response - Tachyphylaxis

Start date: July 2006
Phase: N/A
Study type: Interventional

We are studying the effects of oral water ingestion in patients with orthostatic hypotension. In this study, we are testing the null hypothesis that the blood pressure increase with oral water ingestion will not be diminished if a full prior water dose is given a few hours earlier.