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You must provide a Lead Organiza= tion trial identifier for each trial you register. Optionally, provide a Cl= inicalTrials.gov Identifier.
How to Complete the Tri=
al Identifiers Section
Select or enter the appropriate information in the text fields and drop-= down lists. The following table describes the fields. An asterisk (*) indic= ates a required field.
Instructions for recording Trial Id=
entifiers for Complete trials
Field Label |
Description/Instructions |
---|---|
Lead Organization Trial Identifier* |
Enter the unique identification assigned to t=
he protocol by the sponsoring organization, exactly as it appears in the pr=
otocol document. For Inter-Group trials, type the Lead Group's trial number=
. For multi-site trials that have no assigned single center, use the protoc=
ol ID, for example, |
ClinicalTrials.gov Identifier |
If the trial has been submitted to ClinicalTrials.gov previously, enter = the number assigned to the trial by PRS (ClinicalTrials.gov). The CTRP renamed the previous identifiers "NCT Number" and "NCT ID" to "= ClinicalTrials.gov Identifier". You cannot change the ClinicalTrials.gov Identifier once you have a= dded it. If you need to make changes thereafter, contact the CTRO at = NCICTRO@mail.nih.gov.
When you submit the trial, the system checks the ClinicalTrials.gov iden= tifier you entered to ensure that no other registered trial has the same on= e. The system displays an error message if it finds another trial with the = same ClinicalTrials.gov identifier. If this occurs, check the number you en= tered and try again. If you are certain that the number you entered is corr= ect, contact the CTRO at NCICTRO@mail.nih.gov. |
Other Trial Identifier = td> | Enter an additional trial identifier such as =
unique identifier from other registries, NIH grant numbers, or protocol num=
bers assigned by the Review Board, and then click Add Other Identif=
ier. Repeat this step for each additional identifier. |