Editorials
The rights of patients in research
BMJ 1995; 310 doi: https://doi.org/10.1136/bmj.310.6990.1277 (Published 20 May 1995) Cite this as: BMJ 1995;310:1277Related articles
- RESEARCH Published: 09 January 2006; BMJ doi:10.1136/bmj.38675.677963.3A
- Research Published: 26 January 2006; BMJ 332 doi:10.1136/bmj.38675.677963.3A
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- Incorporating patients perspectives into the initial stages of core outcome set development: a rapid review of qualitative studies of type 2 diabetes
- Parent, patient and clinician perceptions of outcomes during and following neonatal care: a systematic review of qualitative research
- Core Outcome Sets
- From plans to actions in patient and public involvement: qualitative study of documented plans and the accounts of researchers and patients sampled from a cohort of clinical trials
- Sharing Study Results With Trial Participants: Time for Action
- Receiving a summary of the results of a trial: qualitative study of participants' views
- Informing research participants of research results: analysis of Canadian university based research ethics board policies
- Development, validation, and evaluation of the PBC-40, a disease specific health related quality of life measure for primary biliary cirrhosis
- Parallel experience: how art and art theory can inform ethics in human research
- Involving patients in clinical research
- Reactions of participants to the results of a randomised controlled trial: exploratory study
- Lay perspectives: advantages for health research
- Are Proxy Assessments of Health Status After Stroke With the EuroQol Questionnaire Feasible, Accurate, and Unbiased?
- Consumer participation in research and health care
- Obtaining informed consent for neonatal randomised controlled trials---an "elaborate ritual"?
- Details of patients' consent in studies should be reported
- Why don't cancer patients get entered into clinical trials? Experience of the Sheffield Lymphoma Group's collaboration in British National Lymphoma Investigation studies
- Participants should be given feedback about the trial
- Training in substance abuse is lacking for GPs
- Patients often present too late for inclusion in trials