For Clinical trials we have terms and definitions in 14 topics. The topics are Bioinformatics, Biology, Breast Cancer, Cholesterol, Colorectal and Pelvic Floor Diso, Evidence Based Medicine, Food, Food and Health, Gynecological, Gynecology, Health, Hepatitis B, Oncology and Prostate Cancer.

Research studies that involve patients. Biotechnology companies typically use clinical trials to assess the efficacy and safety of new therapies and to answer scientific questions. Typically, there are 3 phases during a clinical trial. Phase I is designed to evaluate the safety of the product in humans; phase II analyses the effects of dose escalation, and phase III definitively evaluates the clinical efficacy of the product.
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The last phase in the development process for new drugs in order to determine the effect on patients in real life studies.
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Organized research studies that provide clinical data for assessment of a new treatment or drug.
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Trials to evaluate the effectiveness and safety of medications or medical devices by monitoring their effects on large groups of people.
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Research studies that involve patients. Each study is designed to find better ways to prevent, detect, diagnose, or treat diseases and to answer scientific questions.
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Randomization, Sample, Control group, Randomized Controlled Trial (RCT), Cohort Study, Case-Control Study, Cross-sectional study, Crossover Study Design, Case Series, Case Report, Double-blind, Intention-to-Treat Analysis.
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Inical trials undertake experimental study of human subjects. ials may attempt to determine whether the finds of basic research are applicable to humans, or to confirm the results of epidemiological research. udies may be small, with a limited number of participants, or they may be large intervention trials that seek to discover the outcome of treatments on entire populations. e "gold standard" clinical trials are double-blind, placebo-controlled studies which employ random assignment of subjects to experimental and control groups unknown to the subject or the researcher.
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Clinical trials undertake experimental study of human subjects. Trials may attempt to determine whether the finds of basic research are applicable to humans, or to confirm the results of epidemiological research. Studies may be small, with a limited number of participants, or they may be large intervention trials that seek to discover the outcome of treatments on entire populations. The "gold standard" clinical trials are double-blind, placebo-controlled studies which employ random assignment of subjects to experimental and control groups unknown to the subject or the researcher.
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Organized research studies that provide clinical data aimed at finding better ways to prevent, detect, diagnose, or treat diseases.
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Organized research studies that provide clinical data aimed at finding better ways to prevent, detect, diagnose, or treat diseases.
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Organized research studies that provide clinical data aimed at finding better ways to prevent, detect, diagnose, or treat diseases.
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Carefully controlled studies that are conducted in humans who volunteer to test the effectiveness and safety of new drugs, medical products or techniques. All drugs in the United States undergo three phases of clinical trials before being approved for general use.
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Studies that evaluate new drugs or new types of treatment.
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Studies conducted with cancer patients, usually to evaluate a promising new treatment. Each study is designed to answer questions to find better ways to treat patients.
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