The following table lists and describes some of the data elements displayed in the Milestone Report for each milestone.
| Data Element | Description |
|---|---|
| NCI ID | The trial to which the milestone applies. The unique ID assigned to the trial by the CTRP. |
| Milestone | The name of the milestone. |
| Milestone Date | The date CTRO added the milestone. |
| User Name | The CTRO user who added the milestone. |
| Submission Type | The submission type of the trial to which the milestone applies, whether the trial is an original submission or an amendment. |
Trial Category | The category of the trial to which the milestone applies. category of the trial, as determined by the submission of a full protocol (Complete) or a ClinicalTrials.gov import (Abbreviated). |
| No of Submission | The submission to which the milestone applies, as a number identifying the trial record in the sequence of submissions for that trial. An original submission is submission 1. |
Trial/Study Type | The primary investigative techniques used in the protocol (interventional or non-interventional). The non-interventional category includes observational and ancillary/correlative studies. For information, refer to Trial Types and Subtypes. |
Trial Sub Type | The trial subtype: observational or ancillary/correlative. A subtype is available only for non-interventional trials. For information, refer to Trial Types and Subtypes. |
Primary Purpose | The main reason for conducting the trial. |
Primary Purpose Other Text | Any text entered for the trial, as a detailed description of the trial’s primary purpose, if the primary purpose is Other. |
Secondary Purpose | The secondary reason for conducting the trial. |
Secondary Purpose Other Text | Any text entered for the trial, as a detailed description of the trial’s secondary purpose, if the secondary purpose is Other. |
| Lead Organization | The lead organization on the trial to which CTRO added the milestone. name of the organization responsible for the trial's research protocol, and responsible for the overall scientific and administrative coordination, study monitoring, and data management activities of the trial. |
| Comments | Any comments that have been entered for the milestone. |
