Table 1.
Benefits of research registration.
| Stakeholder | Benefit |
|---|---|
| Research and clinical community | ❖ Reduce publication and reporting bias (not all studies performed are published – especially negative studies) ❖ Increase transparency ❖ Identify on-going studies in their field – the cutting edge and gaps ❖ Aids research quality – allows for open and early peer-review of study objectives and methods and their refinement ❖ Aids guideline development and evidence synthesis/systematic review ❖ global collaboration between researchers – more multicentre studies |
| Editors and peer-reviewers | ❖ Compare study findings with registered study protocol ❖ Evidence-based medicine |
| Commissioners, funders and wider society | ❖ Reduce unnecessary duplication saving funds |
| Institutions | ❖ Increased collaboration – research that's more global, multicentre and more interdisciplinary |
| Patients and the public | ❖ Can find out about research of interest to them (e.g. HIV treatments) ❖ Respect, dignity and ethics – people who enter studies expect a permanent record of it. |