CR ImageCIOD
PatientMModule - Patient
Clinical Trial SubjectUModule - Patient
General StudyMModule - Study
Patient StudyUModule - Study
Clinical Trial StudyUModule - Study
(0012,0050) Clinical Trial Time Point ID2Long String
(0012,0051) Clinical Trial Time Point Description3Short Text
(0012,0052) Longitudinal Temporal Offset from Event3Double
(0012,0053) Longitudinal Temporal Event Type1CCode String
(0012,0083) Consent for Clinical Trial Use Sequence3Sequence
(0012,0020) Clinical Trial Protocol ID1CLong String
(0012,0084) Distribution Type1CCode String
(0012,0085) Consent for Distribution Flag1Code String
General SeriesMModule - Series
CR SeriesMModule - Series
Clinical Trial SeriesUModule - Series
General EquipmentMModule - Equipment
General ImageMModule - Image
General ReferenceUModule - Image
Image PixelMModule - Image
Contrast/BolusCModule - Image
Display ShutterUModule - Image
DeviceUModule - Image
SpecimenUModule - Image
CR ImageMModule - Image
Overlay PlaneUModule - Image
Modality LUTUModule - Image
VOI LUTUModule - Image
SOP CommonMModule - Image
Common Instance ReferenceUModule - Image
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Multi-frame True Color SC ImageCIOD
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X-Ray Radiofluoroscopic ImageCIOD
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RT DoseCIOD
RT Structure SetCIOD
RT PlanCIOD
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VL Whole Slide Microscopy ImageCIOD
Real-Time Video Endoscopic ImageCIOD
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Grayscale Softcopy Presentation StateCIOD
Color Softcopy Presentation StateCIOD
Pseudo-Color Softcopy Presentation StateCIOD
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Basic Structured DisplayCIOD
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Basic Text SRCIOD
Enhanced SRCIOD
Comprehensive SRCIOD
Key Object Selection DocumentCIOD
Mammography CAD SRCIOD
Chest CAD SRCIOD
Procedure LogCIOD
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Spectacle Prescription ReportCIOD
Colon CAD SRCIOD
Macular Grid Thickness and Volume ReportCIOD
Implantation Plan SR DocumentCIOD
Comprehensive 3D SRCIOD
Radiopharmaceutical Radiation Dose SRCIOD
Extensible SRCIOD
Acquisition Context SRCIOD
Simplified Adult Echo SRCIOD
Patient Radiation Dose Structured ReportCIOD
Planned Imaging Agent Administration SRCIOD
Performed Imaging Agent Administration SRCIOD
Rendition Selection DocumentCIOD
Enhanced MR ImageCIOD
MR SpectroscopyCIOD
Enhanced MR Color ImageCIOD
Raw DataCIOD
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Spatial RegistrationCIOD
Deformable Spatial RegistrationCIOD
Spatial FiducialsCIOD
Ophthalmic Photography 8 Bit ImageCIOD
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Stereometric RelationshipCIOD
Hanging ProtocolCIOD
Encapsulated PDFCIOD
Encapsulated CDACIOD
Real World Value MappingCIOD
Enhanced XA ImageCIOD
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RT Ion PlanCIOD
RT Ion Beams Treatment RecordCIOD
SegmentationCIOD
Ophthalmic Tomography ImageCIOD
X-Ray 3D Angiographic ImageCIOD
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Lensometry MeasurementsCIOD
Autorefraction MeasurementsCIOD
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Intraocular Lens CalculationsCIOD
Generic Implant TemplateCIOD
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RT Beams Delivery InstructionCIOD
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Tractography ResultsCIOD
RT Brachy Application Setup Delivery InstructionCIOD
Planar MPR Volumetric Presentation StateCIOD
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CT Performed Procedure ProtocolCIOD
CT Defined Procedure ProtocolCIOD
Protocol ApprovalCIOD
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Ophthalmic Optical Coherence Tomography B-scan Volume AnalysisCIOD
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Basic DirectoryCIOD

Built with by Innolitics, a team of medical imaging software developers.

Data synced with official DICOM standard on 12 May 2020. The DICOM Standard is under continuous maintenance, and the current official version is available at http://www.dicomstandard.org/current/. DICOM Parts 3, 4, and 6, © NEMA. Please note that the most recent PDF version of the standard is the official reference, and should checked when making technical decisions.

Clinical Trial Protocol ID Attribute

Tag(0012,0020)
TypeConditionally Required (1C)
KeywordClinicalTrialProtocolID
Value Multiplicity1
Value RepresentationLong String (LO)
Example Values
  • UCSF_PILOT
  • 6668
  • 6688

The identifier of the protocol for which consent to distribute has been granted.

Required if Distribution Type (0012,0084) is NAMED_PROTOCOL and the protocol is not that which is specified in Clinical Trial Protocol ID (0012,0020) in the Clinical Trial Subject Module.

Clinical Trial Subject Module

C.7.1.3 Clinical Trial Subject Module

Table C.7-2b contains Attributes that identify a Patient as a clinical trial or research Subject.

Table C.7-2b. Clinical Trial Subject Module Attributes

Attribute Name

Tag

Type

Attribute Description

Clinical Trial Sponsor Name

(0012,0010)

1

The name of the clinical trial or research sponsor. See Section C.7.1.3.1.1.

Clinical Trial Protocol ID

(0012,0020)

1

Identifier for the noted protocol. See Section C.7.1.3.1.2.

Clinical Trial Protocol Name

(0012,0021)

2

The name of the clinical trial or research protocol. See Section C.7.1.3.1.3.

Clinical Trial Site ID

(0012,0030)

2

The identifier of the site responsible for submitting clinical trial or research data. See Section C.7.1.3.1.4.

Clinical Trial Site Name

(0012,0031)

2

Name of the site responsible for submitting clinical trial or research data. See Section C.7.1.3.1.5

Clinical Trial Subject ID

(0012,0040)

1C

The assigned identifier for the clinical trial or research subject. See Section C.7.1.3.1.6. Shall be present if Clinical Trial Subject Reading ID (0012,0042) is absent. May be present otherwise.

Clinical Trial Subject Reading ID

(0012,0042)

1C

Identifies the subject for blinded evaluations. Shall be present if Clinical Trial Subject ID (0012,0040) is absent. May be present otherwise. See Section C.7.1.3.1.7.

Clinical Trial Protocol Ethics Committee Name

(0012,0081)

1C

Name of the Ethics Committee or Institutional Review Board (IRB) or Institutional Animal Care and Use Committees (IACUC) responsible for approval of the Clinical Trial or research. Required if Clinical Trial Protocol Ethics Committee Approval Number (0012,0082) is present.

Clinical Trial Protocol Ethics Committee Approval Number

(0012,0082)

3

Approval number issued by committee described in Clinical Trial Protocol Ethics Committee Name (0012,0081).


C.7.1.3.1 Clinical Trial Subject Attribute Descriptions

Identification of subjects in clinical trials or research generally requires a combination of the following four Attributes:

  1. Clinical Trial Sponsor Name (0012,0010),

  2. Clinical Trial Protocol ID (0012,0020),

  3. Clinical Trial Subject ID (0012,0040) (or Clinical Trial Subject Reading ID (0012,0042) for blinded evaluations), and

  4. Clinical Trial Site ID (0012,0030).

For trials in which subject identifiers are unique within the scope of the Clinical Trial Protocol (e.g., if subject identifiers are centrally assigned or contain the site identifier) the Clinical Trial Site ID (0012,0030) is not required to identify subjects.

C.7.1.3.1.1 Clinical Trial Sponsor Name

The Clinical Trial Sponsor Name (0012,0010) identifies the entity responsible for conducting the clinical trial or research and for defining the Clinical Trial Protocol ID (0012,0020).

C.7.1.3.1.2 Clinical Trial Protocol ID

The Clinical Trial Protocol ID (0012,0020) is the number or character sequence used by the Clinical Trial Sponsor to uniquely identify the investigational protocol in which the subject has been enrolled.

C.7.1.3.1.3 Clinical Trial Protocol Name

The Clinical Trial Protocol Name (0012,0021) contains the title of the investigational protocol in which the subject has been enrolled.

Note

It is recommended that the phase of the clinical trial or research be noted in the Clinical Trial Protocol Name, if applicable.

C.7.1.3.1.4 Clinical Trial Site ID

The Clinical Trial Site ID (0012,0030) is the identification number or character string (issued by the entity identified by the Clinical Trial Sponsor Name (0012,0010)) used to identify the site responsible for submitting clinical trial or research data.

C.7.1.3.1.5 Clinical Trial Site Name

The Clinical Trial Site Name (0012,0031) is a character string used to identify the site responsible for submitting clinical trial or research data.

C.7.1.3.1.6 Clinical Trial Subject ID

The Clinical Trial Subject ID (0012,0040) identifies the subject within the investigational protocol specified by Clinical Trial Protocol ID (0012,0020).

Note

The Clinical Trial Subject ID (0012,0040) may, but is not required to be, the same as Patient ID (0010,0020).

C.7.1.3.1.7 Clinical Trial Subject Reading ID

The Clinical Trial Subject Reading ID (0012,0042) identifies the subject in the context of blinded evaluations.