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A Phase II Study of Risk-Adapted IV Melphalan in Patients with AL (Primary systemic) Amyloidosis
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A double-blind, randomised, placebo controlled crossover study on the effects of 100mg, three times daily, Z-338 on the symptomatic response to a nutrient challenge and gasteric nutrient distribution and emptying in subjects with and without functional dyspepsia.
Zeria Pharmaceutical Co. Ltd is studying an investigational drug called Z-338. This drug is not available for sale in the United States or Australia. Z-338 is being studied as a possible treatment for functional dyspepsia (FD). FD is a disease that causes various abdominal symptoms such as fullness, stomach pain, nausea, early satiety and bloating.
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Phase I dose-escalation study for CYT997
CYT997 is an experimental anticancer agent with vascular targetting activity. This Phase I trial aims to determine the safety and tolerability of CYT997 when given as a 24-hour intravenous infusion.
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First line irinotecan dose escalation study
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Deep breaths and airway closure in asthma
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Post Discharge Care for High-Risk Psychiatric Patients
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The Role of non-GP Staff in Chronic Disease Management in General Practice.
This is a randomised clinical trial that tests the efficacy of a general practice based intervention to enhance the role of non-GP staff including practice managers, practice nurses and receptionists in chronice diesease management in general practice in terms of its impact on the quality and outcome of care for patients with diabetes and/or ischaemic heart disease and/or hypertension. Key primary measures include an audit of medical records, 20-item patient Assessment of Chronic Illness Care (PACIC), SF-12 (v2), and practice claims of HIC patment for long consultations (Levels C & D), care plans, completed cycles of care, investigations (HbAIc, urinary micro albumin) and eye referral for diabetes and the quality of clinical care measured by clinical care interview. Secondary outcome measures include Team Climate Inventory, the Staff Roles Interview, and a practice profiling survey of practice systems for chronic disease care. These measures will be taken at baseline, 6 and 12 months from baseline.
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Comparison of a single dose of intravenous paracetamol with rectal paracetamol and placebo in the treatment of mild to moderate postoperative pain
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A Phase II Study of Abatacept Versus Placebo to Assess the Prevention of Rheumatoid Arthritis (RA) in Adult Patients With Undifferentiated Arthritis Who Are at High Risk for the Development of RA
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A Phase IIIB Multi-Center, Randomized, Double-Blind Study to Evaluate Remission and Joint Damage Progression in Methotrexate Naive Early Erosive RA Subjects Treated With Abatacept Plus Methotrexate Compared With Methotrexate