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Verified by University of Texas Southwestern Medical Center, February 2008 Read More...
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The purpose of this trial is to evaluate the physical function outcomes in anemic, critically ill, trauma subjects treated with epoetin alfa (PROCRIT®) compared to placebo. Read More...
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The primary objective of this study is to compare the effect of giving PROCRIT (Epoetin alfa) to patients before, during and after elective major abdominal surgery (perioperatively) to that of patients receiving Standard of Care (SOC) on the proportion...
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This study was a Phase I, open label, randomized, 2-period, 2-sequence, crossover study designed to assess the relative bioavailability of Saizen administered by the ATS-1 needle-free injection device and a standard needle and syringe. Informed consent...
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This study has 4 phases: screening phase (visit 1), treatment phase (visit 2 - 6 mths after treatment initiation), and end of treatment phase (visit 3 - end of year 1). Only in the case a serious adverse event (SAE) arises, will there be a follow up phase...
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The purpose of this investigation is to evaluate the effectiveness of an investigational device which is similar in appearance to a "tanning bed" but which emits ultraviolet irradiation of a specific wavelength known as UVA1. This device has...
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To study further the association between blood pressure mortality among those who participated in both the Hypertension Detection and Follow-up Program (HDFP) screen and the East Boston Established Populations for Epidemiologic Studies in the Elderly...
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To compare the effects of two stress reduction techniques, Transcendental Meditation (TM) and Progressive Muscle Relaxation (PMR), on the control of mild hypertension in elderly Blacks with hypertension. Read More...
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To re-examine the relationship between suppressed anger, elevated blood pressure and all-cause as well as coronary heart disease (CHD) mortality using data from the Life Change Event Study (LCES) conducted on a representative sample of the Tecumseh Community...
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Our hypotheses are that HBIEP will improve cancer-related insomnia and decrease cancer-related fatigue. The study is a randomized trial with repeated measures of 200 patients receiving high dose chemotherapy as treatment for multiple myeloma. Data analysis...
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Verified by Southern California University of Health Sciences, January 2008 Read More...
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The aim of the present study is to identify changes in the cardiovascular system in patients with pulmonary hypertension (PH) by magnetic resonance imaging (MRI). MRI is accepted as golden standard method for the evaluation of left and right ventricular...
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The primary objective of this study is to evaluate the safety and efficacy of ambrisentan in a broad population of subjects with pulmonary hypertension. Secondary objectives of this study are to evaluate the effects of ambrisentan on other clinical measures...
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AMB-320/321-E has been designed to provide long-term, controlled monitoring of PAH patients treated with ambrisentan in order to properly define the adverse event profile associated with this ERA, including the incidence and severity of elevated serum...
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Verified by National Institutes of Health Clinical Center (CC), March 2008 Read More...
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