UQ Research support: Clinical trials
- Clinical trialsThe information on this page relates to clinical trial requirements of the University of Queensland. If you are conducting a clinical trial it is important that you understand your role and responsibilities, and you familiarize with the UQ Clinical trial governance procedure.
Appraisal of clinical guidelines
- AGREE IIAGREE II is an international tool to assess the quality and reporting of practice guidelines.
Reporting health research
- PRISMAPRISMA stands for Preferred Reporting Items for Systematic Reviews and Meta-Analyses. It is an evidence-based minimum set of items for reporting in systematic reviews and meta-analyses.
Patents
- Derwent innovations indexMerges patent information from Derwent World Patents Index with patent citation information from the Derwent Patents Citation Index.
See our guide to finding patents:
Clinical trial checklists
Reporting clinical trials:
Assessing the validity of clinical trials:
Evidence-based medicine: how to practice and teach it by Publication Date: 2010Includes checklists to assist with the assessment of the validity of clinical trials.
Policy statements and guidelines for registration of trials
- Australian New Zealand Clinical Trials RegistryANZCTR includes trials from pharmaceuticals, surgical procedures, preventive measures, lifestyle, devices, treatment and rehabilitation strategies and complementary therapies. It was established at the NHMRC Clinical Trials Centre.
- Is this Clinical trial fully registered?A statement from the International Committee of Medical Journal Editors (N Engl J Med 2005; 352:2436-2438June 9, 2005DOI: 10.1056/NEJMe058127)
- International Clinical Trials Registry PlatformICTRP is managed by the World Health Organization and is a central database of all intervention trials that are registered in their partner registries.
- CONSORT StatementAn important research tool that takes an evidence-based approach to improve the quality of reports of randomized trials. The CONSORT statement provides revised recommendations for improving the quality of reports of parallel-group randomised trials.
- PhRMA Principles on conduct of Clinical trials and communication of Clinical trial resultsPharmaceutical Research and Manufacturers of America