CONSORT Plus Guideline: Administration

University of California San Francisco

Here are the required and recommended information to be reported about a trial's administration. The bolded items are part of the Minimal Data Set.

Click on Descriptor Name for an example of the item.

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Administration

Heading	Required Items	Recommended Items	Optional Items
Study Names	Study name Official abbreviation
Investigators	Names and institutions (including principal investigator) Investigator contributions Group authorship name	Investigator addresses	Specialties of investigators
Ethics	IRB approval? Informed consent obtained?	Who obtained consent	From whom consent obtained
Contact Person	Name of contact person Contact address and details
Funding	Funder names Funder types	Description of funder review of manuscripts	Start and end date of funding
Oversight Committees		Committee names Committee tasks	Names of committee chairs Background and training of members
Study Sites	Study site names Study site locations	Study site principal investigators Brief description of study sites	Sites withdrawn from particiption Sites added to original protocol
Stage of Trial	Current stage of trial

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