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NCT ID: NCT00775749 Withdrawn - Clinical trials for Postoperative Nausea and Vomiting

Transdermal Nicotine in Female Patients at High Risk for Post Operative Nausea and/or Vomiting (PONV)

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

The purpose of this study is to see if the nicotine patch reduces post operative nausea and/or vomiting (PONV) among non-smoking patients who are at high risk of PONV.

NCT ID: NCT00775554 Withdrawn - Forearm Fracture Clinical Trials

Comparison Study of Using Ultrasound Guidance for Hematoma Blocks vs. Traditional Approach

Start date: September 2008
Phase: N/A
Study type: Interventional

Will use visual analog scales to compare effectiveness of traditional hematoma block vs ultrasound guided hematoma block with regards to pain. This will be done for closed forearm fractures.

NCT ID: NCT00774891 Withdrawn - Ischemia Clinical Trials

Comparison Of Left Ventricular Volume And Wall Stress With Dobutamine And Exercise Echocardiography

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

This study will compare the physiologic responses between exercise stress echocardiography and pharmacologic stress echocardiography on left ventricular volume and wall stress.

NCT ID: NCT00774657 Withdrawn - Aortic Stenosis Clinical Trials

Ventricular Remodeling In Patients With Aortic Stenosis Assessed Echocardiography

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

This preliminary study will compare the effectiveness of two-dimensional and three-dimensional echocardiographic measurements of wall thickness and left ventricular mass in patients with Aortic Stenosis

NCT ID: NCT00773552 Withdrawn - Overactive Bladder Clinical Trials

Solifenacin Succinate Versus Placebo in Inner City Women Ages 20-45 With Overactive Bladder

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

In this study we hope to establish the prevalence of urinary urge symptoms (with or without incontinence) in a multicultural, underserved, hospital clinic population in women between the ages of 20 and 45. Quality of life (QOL) in these individuals will be examined. The goal is to show a 15% reduction in number of voids in a 24 hour period in our study population after 12 weeks of treatment with solifenacin succinate. Hypothesis: We believe that urinary urge symptoms are under-reported in young women and believe they pose a significant strain on quality of life on otherwise young, healthy individuals. Treatment with solifenacin succinate will improve symptoms, in turn improving QOL for these individuals.

NCT ID: NCT00773084 Withdrawn - Clinical trials for Diastolic Heart Failure

Aliskiren and Renin Inhibition in Diastolic Heart Failure

ARID-HF
Start date: September 2008
Phase: N/A
Study type: Interventional

This study is being conducted to compare the effects that 2 different combinations of heart failure medications have on the levels of certain blood markers which cause and/or worsen heart failure. Additionally, the investigators will investigate any differences that may exist between Hispanics and Non-Hispanics. The investigators hope to find that Hispanic Americans will have a greater response to this new regimen compared to non-Hispanic Americans.

NCT ID: NCT00770705 Withdrawn - Clinical trials for Congenital Heart Disease

Parenteral Phenoxybenzamine During Congenital Heart Disease Surgery

Start date: October 2008
Phase: Phase 2
Study type: Interventional

Phenoxybenzamine, an irreversible alpha-adrenergic blocker, may prove beneficial to infants and children with congenital heart disease undergoing open cardiac repair, due to a theoretic benefits of a uniform and smooth reduction in systemic vascular resistance in the perioperative period. Vasodilation allows for low pressure, high flow systemic perfusion while on cardiopulmonary bypass. Support for the use of phenoxybenzamine in humans has been documented in several studies involving the perioperative management of both adults and children requiring cardiopulmonary bypass, and in management of patients with pheochromocytoma. 1-7 Phenoxybenzamine has been associated with more uniform body cooling and rewarming, and improved tissue perfusion during bypass.8 It is also known to increase cardiac output, stroke volume, and renal blood flow when given intravenously. 9 Specifically in pediatric open heart surgery, the combined use of phenoxybenzamine and dopamine provided a stable hemodynamic condition without a high total peripheral vascular resistance and stimulated postoperative diuresis. 9 Afterload reduction with parenteral phenoxybenzamine in neonates undergoing the Norwood procedure for hypoplastic left heart syndrome is associated with improved systemic oxygen delivery and stabilization of systemic vascular resistance.10 Furthermore, a strategy of reducing afterload with phenoxybenzamine and stabilizing the pulmonary to systemic flow ratio in this select population of patients has also been shown to improve operative survival. 11 We hypothesize that phenoxybenzamine will reduce afterload on the systemic ventricle in our selected patient population, thereby improving ventricular performance and decreasing the risks of pulmonary to systemic flow imbalance associated with current short-acting vasodilator therapy. We will plan to evaluate both physiologic variables as well as surgical outcomes in the selected study population.

NCT ID: NCT00769925 Withdrawn - Anxiety Disorders Clinical Trials

Assessing Different Methods of Anxiety Care in Pediatric Settings

Start date: November 2008
Phase: N/A
Study type: Interventional

This study will compare the effectiveness of delivering cognitive behavioral therapy for children with anxiety disorders through in-person contact versus through workbooks and telephone communication.

NCT ID: NCT00769834 Withdrawn - Clinical trials for Chronic Kidney Disease

Disc Edema in Patients With Chronic Kidney Disease

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

Papilledema is defined as swelling of the optic nerves often due to increased intracranial pressure. When present, it often indicates life-threatening lesions of the brain such as tumors, abscesses, meningitis, encephalitis, venous sinus obstruction or intracranial hemorrhage. A similar clinical picture can also be caused by other conditions such as malignant hypertension, diabetic papillopathy and uremia. When the intracranial pressure is elevated in the absence of any known cause then it is called Idiopathic Intracranial Hypertension (IIH). Untreated papilledema can cause progressive optic nerve damage and blindness. Patients with chronic kidney disease have a number of co-morbidities and thus are at an increased risk for developing papilledema. Although clinicians have observed that patients with kidney diseases have increased incidence of papilledema (unpublished data by Corbett et al), there have been no studies on this subject to date. We believe that a higher incidence of papilledema is found in patients with kidney diseases and this study could provide evidence to suggest routine ophthalmic screening in this patient group. Hypothesis: The prevalence of optic disc swelling is increased in patients with chronic kidney disease. Purpose: To establish the prevalence of disc edema in patients with chronic kidney disease.

NCT ID: NCT00768131 Withdrawn - Clinical trials for Carcinoma, Non-Small-Cell Lung

A Study to Determine Whether EGFR Status by FISH Can Predict Results in Non Small Cell Lung Cancer (NSCLC) Patients Treated With Cetuximab, Carboplatin and Paclitaxel

Start date: October 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if EGFR status (positive or negative) by FISH can predict response to cetuximab therapy in NSCLC patients treated with carboplatin and paclitaxel