Results 191 to 200 of about 1,240,122 (231)
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What are the four phases of clinical research trials?
BMJ, 2014Children with neurological and developmental disorders often experience chronic sleep disturbances. Melatonin has been commonly prescribed because of its hypnotic properties. However, trials have had conflicting results. Therefore, researchers assessed the effectiveness of melatonin in treating severe sleep problems in children with neurodevelopmental ...
P. Sedgwick
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The Drug Development Process and the Phases of Clinical Research
2007A. Bacchieri, G. Cioppa
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A Brief Introduction to Phases of Clinical Medical Research for the SOF Medic
Journal of Special Operations Medicine, 2021This is the first of an ongoing series to provide a background into reading medical research literature for the SOF medic.
Alex, Merkle, Josh, Randles
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Enhancing Traceability in Clinical Research Data through a Metadata Framework
Methods of Information in Medicine, 2020Background The clinical research data lifecycle, from data collection to analysis results, functions in silos that restrict traceability. Traceability is a requirement for regulated clinical research studies and an important attribute of nonregulated ...
Sam Hume +2 more
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Continuity of Physician Participation in Phase I Clinical Research
Drug Information Journal, 1994As the competition for research dollars becomes more keen, contract research organizations (CROs) are evolving into larger entities. As a result, Phase I units affiliated with CROs have grown in size andpersonnel in order to accommodate multiple studiesperformedsimultaneously.
Philip M. Brown +2 more
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‘Risky’ research and participants' interests: the ethics of phase 2C clinical trials
Clinical Ethics, 2011Biomedical research involving human participants is highly regulated and subject to stringent ethical requirements. Clinical research ethics, regulation and policy have tended to focus almost exclusively on the protection of participants' interests against harms that might result from taking part in research.
Chan, Sarah +3 more
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Journal of Empirical Research on Human Research Ethics
Clinical studies are reviewed by clinical research ethics committees (CRECs) in order to ensure that they are conducted within the framework of good clinical practice and that the rights of volunteers are respected.
Gungor Buket
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Clinical studies are reviewed by clinical research ethics committees (CRECs) in order to ensure that they are conducted within the framework of good clinical practice and that the rights of volunteers are respected.
Gungor Buket
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Cancer, 2023
AbstractBackgroundAlthough most patients with cancer are treated with local therapy (LT), the proportion of late‐phase clinical trials investigating local therapeutic interventions is unknown. The purpose of this study was to determine the proportion, characteristics, and trends of phase 3 cancer clinical trials assessing the therapeutic value of LT ...
Alexander D. Sherry +13 more
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AbstractBackgroundAlthough most patients with cancer are treated with local therapy (LT), the proportion of late‐phase clinical trials investigating local therapeutic interventions is unknown. The purpose of this study was to determine the proportion, characteristics, and trends of phase 3 cancer clinical trials assessing the therapeutic value of LT ...
Alexander D. Sherry +13 more
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The Complexity of Consenting to Clinical Research in Phase I Pediatric Cancer Studies
Pediatric Drugs, 2015The principal aim of phase I studies is to define the recommended dosing of drugs for phase II studies through assessment of drug pharmacokinetics and observation of the drug's toxicity profile. In the setting of pediatric oncology, the use of an experimental drug in phase I study is offered when prognosis is poor.
Tal, Schechter, Ronald, Grant
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