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Clinical Trials
In line with requirements of the International Committee of Medical Journal Editors (http://www.icmje.org/, http://www.icmje.org/faq_clinical.html), Diabetologia requires authors to have registered their trial in an acceptable registry at the time of conception. The registry must:
- be accessible to the public at no charge
- be open to all prospective registrants and managed by a not-for-profit organisation
- be a mechanism to ensure the validity of the registration data
- be electronically searchable
- Australian New Zealand Clinical Trials Registry (www.actr.org.au)
- ClinicalTrials.gov (www.clinicaltrials.gov)
- International Standard Randomised Controlled Trial Number Register (http://isrctn.org)
- UMIN Clinical Trials Registry (www.umin.ac.jp/ctr/index.htm)
- Nederlands Trial Register (www.trialregister.nl/)
- or any registries accepted by WHO as primary registers (see www.who.int/ictrp/network/primary/en/index.html)
The trial registry number should be included at the end of the Abstract.
Randomised control trials Authors should follow the CONSORT statement (see http://www.consort-statement.org/index.aspx?o=1011) and also include a patient flow diagram.