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What Is Yeast Infection Or Candidiasis? What Is Vaginal Thrush?
Vaginal thrush (thrush) is a yeast infection caused by a type of fungus of the candida species, usually Candida albicans. It can affect all women, but is more common among women who are pregnant, those who have weakened immune systems, and women aged 30 to 50. Thrush is generally recurring - it comes back. The fungus, candida albicans, exists naturally in the vagina. As long as it does not multiply too much a woman will not notice it is there. However, if can sometimes multiply to such an extent that it causes swelling of the vagina and vulva.
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MAGI's 2009 Clinical Research Conference - WEST
If you are a clinical research novice or veteran with a study sponsor, research site, or CRO in a corporate, academic or other organization, you will find a comprehensive program that focuses on your current needs and broadens your knowledge. MAGI conferences feature balanced co-presentations from sponsors, sites and CROs, real-life examples, practical tips, and lots of interaction and networking. This year"s conference will feature:
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New Legislation Seeks To Boost Participation In Clinical Trials For Rare Diseases
New legislation introduced would allow patients with rare diseases to participate in clinical drug studies without losing their eligibility for government healthcare coverage.
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Commercialization Grant Awards Announced By Life Sciences Discovery Fund

The Life Sciences Discovery Fund (LSDF) has announced $300,000 in awards from its inaugural winter commercialization grant competition to support commercial translation of health-related technologies by two Washington state-based research teams. Commercialization grants are designed to facilitate the transition of promising ideas or technologies from Washington"s non-profit research sector into marketable products and services that can improve health, foster economic growth, and promote life sciences competitiveness in the state. The grants support proof-of-concept experiments and prototype development activities that are expected to lower the risk of commercialization and help new technologies cross the "valley of death" - that stage of the commercialization pathway where development funding is particularly scarce. One team, led by Philip Fleckman of the University of Washington, will assess the ability of a novel material to prevent infections associated with catheter use. The second team, headed by Kenneth A. Schenkman, also of the University of Washington, will conduct a clinical study of a new device for the early detection of shock. Here are the details of each awarded proposal: Philip Fleckman, University of Washington, $150,000 Project Title: Cutaneous Healing into Porous Biomaterials Impedes Infection Project Focus: To test the ability of a percutaneous catheter to resist infection Percutaneous (skin-penetrating) devices such as vascular and dialysis catheters, glucose monitors, and artificial prostheses are essential for medical care. The use of these critical devices, however, is associated with high risk of infection leading to significant morbidity and mortality. The proposed work is a new approach that uses material into which the skin can heal, thus providing a barrier to microbial attachment and infection. The proposed work will test whether cutaneous integration into biomaterial inserted into the skin will resist bacterial challenge by Staphylococcus aureus, an organism that commonly infects percutaneous devices. The commercialization plan continues a fruitful collaboration with Healionics, a successful start-up biotech company that has licensed the technology from the University of Washington. Kenneth A. Schenkman, University of Washington, $150,000 Project Title: Noninvasive Clinical Monitor for Early Detection of Shock Project Focus: To test a new instrument for the diagnosis and monitoring of shock Shock is a life-threatening medical condition that results in insufficient oxygen reaching body tissues. Early and definitive diagnosis of shock is difficult using current methods. As a result, many cases are missed or not picked up until the critical later stages when organ failure and death may occur. The investigators have developed a novel noninvasive clinical monitor that they believe will fundamentally improve the early detection and continuous monitoring of shock. A proof-of-concept study will be performed on trauma patients upon admission to the emergency department and within the first hours of resuscitation in the intensive care unit. The investigators hope to demonstrate that their new monitor can identify the severity of shock and serve as a sensitive indicator of the adequacy of resuscitation. The commercialization plan for the shock monitor includes the formation of a new start-up company. Funding for the winter commercialization grants comes from donations to LSDF for grant-making purposes by Amgen, the Bill & Melinda Gates Foundation, Group Health Cooperative, Microsoft Corp., the Paul G. Allen Family Foundation, Regence BlueShield, and Safeco Insurance Foundation; and from Washington"s allocation of bonus payments under the Master Tobacco Settlement Agreement of 1998, revenues arising from multi-state litigation with tobacco product manufacturers. Alden Jones Life Sciences Discovery Fund


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