Clinical trials and clinical research are important for the progress of modern medicine. There are five types of clinical trials. Some are paid clinical trials, and some aren't. Learn the types, as well as the different clinical trial phases. Discover th
The principle of respect for patient autonomy and the importance of informed consent are well established in the conduct of clinical research. However, in actual clinical practice, how one applies this concept is not always clear. The provocative results of a randomized trial examining "consolidation...
Physician inoculates patient, hopefully after receiving informed consent. Credit: blakespot, Flickr Making sure that participants of a clinical trial provide informed consent—understanding their role, along with any risks and benefits of voluntary participation—is a cornerstone of ethical trials. Now, ...
In lower-income countries like Ghana, participants are often targeted as preferable, 搂treatment-nave篓 trial candidates, meaning individuals who have not been exposed to drugs that could potentially interfere with clinical trial results (Frimpong-Mansoh 2008; Mbuagbaw et al. 2011; Petryna 2007)....
for example in another research study or in a clinical trial, the data that you provide as part of the PGP may be used, on its own or in combinat... JE Lunshof,J Bobe,J Aach,... - 《Dialogues in Clinical Neuroscience》 被引量: 101发表: 2010年 Attitudes, understanding, and concern...
Taking new drug as an example, clinical trials are broken down into Phase I to Phase IV, with each phase having a different purpose within the trial. Phase I trials involve a small group of people (20-80) and are concerned with determining a safe dose of the drug being studied as well...
Informed consent in clinical trials in critical care: experience from the PAC-Man Study OBJECTIVES: To identify the proportion of critically ill patients able to consent to participation in a randomised controlled trial (RCT) and to assess to ... SE Harvey,D Elbourne,J Ashcroft,... - 《...
The Clinical Investigation Plan (CIP) is the key document in device trials; it is effectively the equivalent of the protocol in a clinical trial. The CIP is defined as follows (ISO, 2003, p. 6): The CIP shall be a document developed by the sponsor and the clinical investigator(s). The...
What constitutes a "clinical trial" is inconsistently defined in the medical literature. With an initiative by Cancer Care Ontario (CCO) to report institutional clinical trials activity across the province of Ontario, Canada, we sought to investigate the
A short communication course for physicians improves the quality of patient information in a clinical trial We investigated whether a short course in communication skills for physicians would improve the quality of informed consent in a randomized clinical adjuva... PS Hietanen,AR Aro,KA Holli,......