Open-access clinical trial registries: the Italian scenario

THE JAMES LIND ALLIANCE APPROACH TO PRIORITY SETTING FOR PROSTATE CANCER RESEARCH: AN INTEGRATIVE METHODOLOGY BASED ON PATIENT AND CLINICIAN PARTICIPATION

(2011) Artitaya Lophatananon et al.   BJU INTERNATIONAL

Adding value to clinical trial registries: insights from Australian Cancer Trials Online, a website for consumers

(2011) Rachel Dear et al.   Clinical Trials

Need to realign patient-oriented and commercial and academic research

(2011) Alessandro Liberati   LANCET

The Quality of Registration of Clinical Trials

(2011) Roderik F. Viergever et al.   PLoS One

Patients’ and clinicians’ research priorities

(2010) Ruth J. Stewart et al.   HEALTH EXPECTATIONS

Das Deutsche Register Klinischer Studien: Begründung, technische und inhaltliche Aspekte, internationale Einbindung

(2009) G. Dreier et al.   Bundesgesundheitsblatt-Gesundheitsforschung-Gesundheitsschutz

Compliance of clinical trial registries with the World Health Organization minimum data set: a survey

(2009) Lorenzo P Moja et al.   Trials

The impact of consumer involvement in research: an evaluation of consumer involvement in the London Primary Care Studies Programme

(2008) K. Wyatt et al.   FAMILY PRACTICE