<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><rec-number>6223</rec-number><ref-type>Journal Article</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Orentlicher, David</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Making Research a Requirement of Treatment : Why We Should Sometimes Let Doctors Pressure Patients to Participate in Research</style></title><secondary-title><style face="normal" font="default" size="100%">Hastings Center Report</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Informed</style></keyword><keyword><style  face="normal" font="default" size="100%">MEDICINE</style></keyword><keyword><style  face="normal" font="default" size="100%">Patients</style></keyword><keyword><style  face="normal" font="default" size="100%">research</style></keyword><keyword><style  face="normal" font="default" size="100%">THERAPEUTICS</style></keyword></keywords><taxonomies><taxonomy><style  face="normal" font="default" size="100%">Informed Consent</style></taxonomy><taxonomy><style  face="normal" font="default" size="100%">Human Research Subjects</style></taxonomy><taxonomy><style  face="normal" font="default" size="100%">Medicine</style></taxonomy></taxonomies><pubtype><style  face="normal" font="default" size="100%">Journal Article</style></pubtype><audience-level><style  face="normal" font="default" size="100%">ug</style></audience-level><dates><year><style  face="normal" font="default" size="100%">2005</style></year></dates><volume><style face="normal" font="default" size="100%">35</style></volume><pages><style face="normal" font="default" size="100%">20-28</style></pages><issn><style face="normal" font="default" size="100%">00930334</style></issn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Argues that there is a need to relax the precautions taken to ensure voluntary participation of subjects in studies involving the comparison of two or more established therapies to see whether one is superior to the alternative(s). Illustration of the concern with standards for informed consent in research; Way to ensure that all patients receive optimal therapy; Importance of concerns about patient trust in medical research.</style></abstract><doi><style face="normal" font="default" size="100%">10.1353/hcr.2005.0083</style></doi><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><accession-num><style face="normal" font="default" size="100%">18472919</style></accession-num><notes><style face="normal" font="default" size="100%">Orentlicher, David 1,2; Affiliation: 1: Indiana University Center for Bioethics 2: Samuel R. Rosen Professor of Law, Indiana University School of Law -- Indianapolis; Source Info: Sep/Oct2005, Vol. 35 Issue 5, p20; Subject Term: MEDICINE -- Research; Subject Term: THERAPEUTICS; Subject Term: INFORMED consent (Medical law); Subject Term: PATIENTS; Subject Term: RESEARCH; NAICS/Industry Codes: 541712 Reseach and Development in the Physical, Engineering, and Life Sciences (except Biotechnology); Number of Pages: 9p; Document Type: Article</style></notes></record></records></xml>