The CTI segment is an optional segment that contains information to identify the clinical trial, phase and time point with which an order or result is associated.
Seq# | Data Element Name | DataType | Usage | Vocabulary | Cardinality | Item # | Length | C.LEN | Flags |
---|---|---|---|---|---|---|---|---|---|
CTI | |||||||||
1 | Sponsor Study ID | EI | R | [1..1] | 01011 | ||||
2 | Study Phase Identifier | CWE | C | [0..1] | 01022 | ||||
3 | Study Scheduled Time Point | CWE | O | [0..1] | 01055 | ||||
4 | Action Code | ID | O | [0..1] | 00816 | [2..2] |
Definition: This field contains the universal identifier for the clinical trial. The coding system is as described in CSR-1 Sponsor Study ID.
Definition: This field identifies the phase of the study that a patient has entered. See CSP-1 Study Phase Identifier for details of coding systems. Refer to Table 0597 - Study Phase Identifier in Chapter 2C for valid values.
Definition: This field identifies a time point in the clinical trial phase. CTI-2 Study Phase Identifier must be valued if CTI-3 Study Scheduled Time Point is valued. Should correspond to CSS-1 Study Scheduled Time Point. Refer to Table 0598 - Study Scheduled Time Point in Chapter 2C for valid values.
Definition: This field reveals the intent of the message. Refer to HL7 Table 0206 - Segment Action Code for valid values.
The action code can only be used when CTI-1 is valued in accordance with the guidance in Chapter 2, Section 2.10.4.2.