Each entity submitting data to ClinicalTrials.gov must adhere to the following terms and conditions, which are intended to ensure the accuracy, currency and validity of the data.

1. Only data on trials approved by the appropriate regulatory authority may be submitted to ClinicalTrials.gov.
2. Notice of recruiting status changes must be done immediately, and all submitted data must be reviewed, verified and updated at a minimum of every six months.
3. The submitting organization is responsible for the completeness and accuracy of the data submitted to ClinicalTrials.gov.
4. Trial data must be submitted in English.
5. Previous versions of trial data will be available to the public, although the default view will be the most recent version.

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Sponsor Information The sponsoring organization is the entity with primary responsibility for initiating and conducting the trial(s) to be registered.
Registering IND/IDE Trials?	No Yes
Type of Organization:	-- Select One -- Government Agency Industry University Nonprofit Organization Other
Country:
Organization Name:
Organization Address:
Organization Abbreviations and Acronyms:
Parent Organizations, if any:
Official Representative:
Phone:
Email:
Organization URL (optional):
Funding Organization:
Investigator Information
Investigator Name:
Affiliation (if not the sponsor):
Investigator Phone:
Investigator Email:
Regulatory Information: The regulatory authority may be a national or international health authority, an institutional review board or an ethics committee.
Regulatory Authority:
Regulatory Authority Address:
To the best of my knowledge, the above information is true and correct. Questions about this form and the Protocol Registration System (PRS) may be sent to register@ClinicalTrials.gov.