DICOM Module

Clinical Trial Subject Module

Attributes
16
Required (Type 1 / 1C)
7
Source
PS3.3 §C.7.1.3

Overview

specifies the Attributes of the , which identify a Patient as a clinical trial or research Subject.

Attributes

Type: 1 required (non-zero), 1C required when condition met, 2 required (may be zero-length), 2C conditional, 3 optional.

Attribute Tag Type
Clinical Trial Sponsor Name (0012,0010) 1
Clinical Trial Protocol ID (0012,0020) 1
Issuer of Clinical Trial Protocol ID (0012,0022) 3
Other Clinical Trial Protocol IDs Sequence (0012,0023) 3
Clinical Trial Protocol ID (0012,0020) 1
Issuer of Clinical Trial Protocol ID (0012,0022) 1
Clinical Trial Protocol Name (0012,0021) 2
Clinical Trial Site ID (0012,0030) 2
Issuer of Clinical Trial Site ID (0012,0032) 3
Clinical Trial Site Name (0012,0031) 2
Clinical Trial Subject ID (0012,0040) 1C
Issuer of Clinical Trial Subject ID (0012,0041) 3
Clinical Trial Subject Reading ID (0012,0042) 1C
Issuer of Clinical Trial Subject Reading ID (0012,0043) 3
Clinical Trial Protocol Ethics Committee Name (0012,0081) 1C
Clinical Trial Protocol Ethics Committee Approval Number (0012,0082) 3

Used in 165 CIODs