Registration

Please carefully read this guide, if you have any questions, please contact us.

● Which clinical studies should be registered?

All of studies aim to evaluate the effects on human subjects for interventions include drugs, non-drug treatment, instruments and equipments designed as randomized controlled trial or case-control study, or cohort study, or non controlled study or other any observational studies of prevention and treatment studies, prognosis studies, cause studies and diagnostic tests should be registered.

Attention: the transitional policy of retrospective registration will be closed in December 31, 2008. From the date of January 1, 2009, we will accept the prospective registration only.

● Free registration

Chinese Clinical Trial Registry is a non-benefit organization, any registration is free (no charge). Only those which needs us to work on the improving their design needs to pay for the service, Refer to the standard of other registies the registration fee, the service cost is RMB 1,500 yuan for a trial, extra 500 yuan for those who needs to English translation service.

● Any one according to one of these items can apply to discount or exempt for our servise:

Personal project without any funding

Social welfare or beneficent research project

Project for degree thesis of medical student include graduate student, postgraduate student

Each study applying to discount or exempt for registration will be evaluated by ChiCTR for its scientific and clinical value, and the applicant should to provide testify materials about funding status of the study.

● Steps of registration

At the first, you should to establish your personal account in ChiCTR website then, login and select "Project info", "Project management" at left side, and then select "New" at the right side of the window. You can start application for registration via fill electronic registration form online now.

We will prejudication for whether the suggested project according to the registration criteria;

If there is anything unclear, we will contact the registrant to dicuss or quire them provide necessary data by phone or email;

As the trial to be considered eligible for registration, a registration numer will be released.