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1. Indicate whether or not you require an XML document for registration with ClinicalTrials.gov. The default is Yes. If you select No, you will not be asked to provide regulatory and responsible party information.

2. Select or enter the appropriate information in the text fields and drop-down lists. The following table describes the fields. An asterisk (*) indicates a required field.

   
   Instructions for recording Trial Identifiers for Complete trials
   

   Field Label	Description/Instructions
   Lead Organization Trial Identifier*	Enter the unique identification assigned to the protocol by the sponsoring organization, exactly as it appears in the protocol document. For Inter-Group trials, type the Lead Group's trial number. For multi-site trials that have no assigned single center, use the protocol ID, for example, NSAGP-B-40.
   ClinicalTrials.gov Identifier	If the trial has been submitted to ClinicalTrials.gov previously, enter the number assigned to the trial by PRS (ClinicalTrials.gov). Note The CTRP renamed the previous identifiers "NCT Number" and "NCT ID" to "ClinicalTrials.gov Identifier". Note You cannot change the ClinicalTrials.gov Identifier once you have added it. If you need to make changes thereafter, contact the CTRO at NCICTRO@mail.nih.gov. Anchor 6124 6124 Include Page ClinicalTrials.gov Identifier Validation - Include v4.4 ClinicalTrials.gov Identifier Validation - Include v4.4
   Other Trial Identifier	Enter an additional trial identifier such as unique identifier from other registries, NIH grant numbers, or protocol numbers assigned by the Review Board, and then click Add Other Identifier. Repeat this step for each additional identifier. The ID you added is displayed in the Other Identifier list. To delete an identifier you have added, in the Action Column, click Delete.