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NCT ID: NCT00870376 Withdrawn - Clinical trials for Lower Urinary Tract Symptoms

Studies of Biomarkers in Different Urodynamic Diagnoses of Female Patients With Lower Urinary Tract Symptoms

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

Urodynamic study is an objective method to evaluate female patients with lower urinary tract symptoms (LUTS). However, this method includes place a urinary catheter, thus prevents it as a routine method to evaluate and follow up patients with LUTS. Therefore, it is necessary to find a simple and objective method to help in evaluating female patients with LUTS. Several kinds of biomarker had been reported in diagnosing patients with overactive bladder; however, the sensitivity remained poor. The aim of this study is to find a useful biomarker, biomarkers, or combinations, with the aid of urodynamic study, to objectively and precisely in evaluating the female patients with LUTS.

NCT ID: NCT00873132 Withdrawn - Brain Tumor Clinical Trials

BTC Neuropsychological Database

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

Purpose and Objective: The purpose of this study is to collect data both retrospectively and prospectively, by consent, on subjects seen in the PRTBTC. This information will be useful to the investigators to generate hypotheses for planning further psychosocial and medication intervention studies that will hopefully improve primary brain tumor patients' QOL.

NCT ID: NCT00873886 Withdrawn - Pregnancy Clinical Trials

A Study of the Pharmacology of Oseltamivir (Tamiflu) in Pregnancy

Start date: April 2009
Phase: Phase 1
Study type: Interventional

The primary research question of this study is: Does the pharmacokinetics of oseltamivir after a single oral dose differ between the pregnant and non-pregnant women?

NCT ID: NCT00875602 Withdrawn - Clinical trials for Post Surgical Pat., Medical Pat., Resp. Failure, Car.Arrest, Death

Evaluation of EverOn™ - A Contact-Free System for Measuring Heart Rate, Respiratory Rate and Motion

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

Evaluation of continuous monitoring device on patients Risk during hospitalization and nurse satisfaction level.

NCT ID: NCT00878748 Withdrawn - Clinical trials for Major Depressive Disorder

Study Evaluating Effexor XR in Chinese Subjects With Major Depressive Disorder

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

This primary purpose of this study is to assess the efficacy and safety of Effexor XR in preventing recurrence in Chinese patients with recurrent major depressive disorder (MDD) following a 1-year maintenance treatment after an 8-week acute treatment and a 6-month continuation treatment phases. The study will also collect data on the prevalence and pattern of co-morbid anxiety and somatic symptoms and their impact on the recurrence of depression.

NCT ID: NCT00879112 Withdrawn - Clinical trials for Hypercholesterolemia

Study of MB07811 in Subjects With Hypercholesterolemia

Start date: April 2009
Phase: Phase 2
Study type: Interventional

A Phase 2 randomized, placebo controlled study assessing the efficacy, safety, and tolerability of MB07811 given orally to subjects with primary hypercholesterolemia for 12 weeks followed by a 6-week off drug phase.

NCT ID: NCT00881114 Withdrawn - Clinical trials for Head and Neck Cancer

Study Using Pharmacogenetics to Select Treatment for Head and Neck Cancer

PGx-SELECT
Start date: April 2009
Phase: Phase 2
Study type: Interventional

This is a study for patients with head and neck cancer who will be receiving chemotherapy and radiation therapy for their disease. The purpose of this study is to see if the investigators can use genetic differences between patients to select the right drug to use with radiation therapy. This type of genetic testing is called pharmacogenetics. Currently there are two drugs used to treat head and neck cancer that have provided a benefit when given with radiation compared to radiation alone in previous studies. These two drugs are cisplatin and cetuximab (Erbitux). In this trial, the investigators will test whether genetic differences between patients can be used to pick which drug they should receive. A recent study that looked back to see how well patients with head and neck cancer responded to treatment with cisplatin showed that genetic differences in a few genes were associated with who did and who did not survive their cancer. The investigators are taking that finding and using it to test patients for these genetic differences to determine whether they should receive cisplatin or cetuximab. In other words, the investigators are trying to take what is essentially a flip of the coin choice between these two drugs, and instead use individual patient's genetic differences to make-and hopefully improve- this choice.

NCT ID: NCT00883805 Withdrawn - Clinical trials for Total Hip Arthroplasty

Investigation of Systemic Metal Ion Concentration Following a Ceramic-on-metal Total Hip Arthroplasty

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

This is a pilot study to compare systemic concentrations of cobalt and chromium in patients that have previously undergone total hip arthroplasties with ceramic on metal and metal on metal bearing surfaces.

NCT ID: NCT00886548 Withdrawn - Heart Failure Clinical Trials

Echocardiographic Examination Performed by Nurses in Cardiac Intensive Care Unit

Start date: April 2009
Phase:
Study type: Observational

The purpose of this study is: - To study the clinical usefulness of nurse-performed ultrasound and echocardiographic examinations in a cardiac intensive care unit. - To study reproducibility of nurse-performed ultrasound and echocardiographic examinations in a cardiac intensive care unit. - To study which ultrasound measure that best correlate with the amount of pleural effusion.

NCT ID: NCT00887835 Withdrawn - Clinical trials for Lumbar Facet Disease

A Post-Market Study of Transfacet Lumbar Spine Fixation and Fusion Utilizing the PERPOS™ PLS System

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

The purpose of this study is to utilize the PERPOS™ PLS System for transfacet lumbar spine fixation to evaluate its effect on patients' level of pain, procedural complications and functional status.