CDISC DDF Terminology

Preferred Label : CDISC DDF Terminology;

NCIt related terms : DDF;

Alternative definition : CDISC: The terminology subset that includes terms pertaining to the Clinical Data Interchange Standards Consortium (CDISC) Digital Data Flow (DDF) model.;

NCI Metathesaurus CUI : CL1793774;

Details

Origin ID

C188693;

UMLS CUI

C5708920;

Semantic type(s)
- Intellectual Product [UMLS semantic type]
concept_is_in_subset
- Clinical Data Interchange Standards Consortium Terminology [NCIt concept]
subset_includes_concept
- Active Comparator Arm [NCIt concept]
- Address [NCIt concept]
- Address Full Text [NCIt concept]
- Adhesion Performance Study [NCIt concept]
- Adverse Effect Mitigation Study [NCIt concept]
- After Timing Type [NCIt concept]
- Alcohol Effect Study [NCIt concept]
- Alias Code [NCIt concept]
- Ambulatory Care Facility [NCIt concept]
- Approval [NCIt concept]
- Arm Description [NCIt concept]
- Audio-Videoconferencing [NCIt concept]
- Audioconferencing [NCIt concept]
- Baseline Epoch [NCIt concept]
- Basic Research [NCIt concept]
- Before Timing Type [NCIt concept]
- Bioavailability Study [NCIt concept]
- Biomedical Concept [NCIt concept]
- Biomedical Concept Category [NCIt concept]
- Biomedical Concept Category Code [NCIt concept]
- Biomedical Concept Category Description [NCIt concept]
- Biomedical Concept Category Name [NCIt concept]
- Biomedical Concept Name [NCIt concept]
- Biomedical Concept Property [NCIt concept]
- Biomedical Concept Property Concept Code [NCIt concept]
- Biomedical Concept Property Enabled Indicator [NCIt concept]
- Biomedical Concept Property Name [NCIt concept]
- Biomedical Concept Property Required Indicator [NCIt concept]
- Biomedical Concept Property Response Data Type [NCIt concept]
- Biomedical Concept Reference [NCIt concept]
- Biomedical Concept Surrogate Description [NCIt concept]
- Biomedical Concept Surrogate Reference [NCIt concept]
- Biomedical Concept Synonym [NCIt concept]
- Biosimilarity Study [NCIt concept]
- Blinded Treatment Epoch [NCIt concept]
- Both [NCIt concept]
- Brief Protocol Title [NCIt concept]
- Business Therapeutic Areas [NCIt concept]
- CDISC DDF Activity Attribute Terminology [NCIt concept]
- CDISC DDF Address Attribute Terminology [NCIt concept]
- CDISC DDF Analysis Population Attribute Terminology [NCIt concept]
- CDISC DDF Biomedical Concept Attribute Terminology [NCIt concept]
- CDISC DDF Biomedical Concept Category Attribute Terminology [NCIt concept]
- CDISC DDF Biomedical Concept Property Attribute Terminology [NCIt concept]
- CDISC DDF Biomedical Concept Surrogate Attribute Terminology [NCIt concept]
- CDISC DDF Clinical Study Attribute Terminology [NCIt concept]
- CDISC DDF Code Attribute Terminology [NCIt concept]
- CDISC DDF Encounter Attribute Terminology [NCIt concept]
- CDISC DDF Encounter Type Value Set Terminology [NCIt concept]
- CDISC DDF Endpoint Attribute Terminology [NCIt concept]
- CDISC DDF Endpoint Level Value Set Terminology [NCIt concept]
- CDISC DDF Entities Terminology [NCIt concept]
- CDISC DDF Estimand Attribute Terminology [NCIt concept]
- CDISC DDF Indication Attribute Terminology [NCIt concept]
- CDISC DDF Intercurrent Event Attribute Terminology [NCIt concept]
- CDISC DDF Investigational Interventions Attribute Terminology [NCIt concept]
- CDISC DDF Objective Attribute Terminology [NCIt concept]
- CDISC DDF Objective Level Value Set Terminology [NCIt concept]
- CDISC DDF Organization Attribute Terminology [NCIt concept]
- CDISC DDF Organization Type Value Set Terminology [NCIt concept]
- CDISC DDF Procedure Attribute Terminology [NCIt concept]
- CDISC DDF Protocol Status Value Set Terminology [NCIt concept]
- CDISC DDF Response Code Attribute Terminology [NCIt concept]
- CDISC DDF Schedule Timeline Attribute Terminology [NCIt concept]
- CDISC DDF Scheduled Decision Instance Attribute Terminology [NCIt concept]
- CDISC DDF Scheduled Instance Attribute Terminology [NCIt concept]
- CDISC DDF Study Arm Attribute Terminology [NCIt concept]
- CDISC DDF Study Arm Data Origin Type Value Set Terminology [NCIt concept]
- CDISC DDF Study Design Attribute Terminology [NCIt concept]
- CDISC DDF Study Design Population Attribute Terminology [NCIt concept]
- CDISC DDF Study Element Attribute Terminology [NCIt concept]
- CDISC DDF Study Epoch Attribute Terminology [NCIt concept]
- CDISC DDF Study Identifier Attribute Terminology [NCIt concept]
- CDISC DDF Study Protocol Version Attribute Terminology [NCIt concept]
- CDISC DDF Timing Attribute Terminology [NCIt concept]
- CDISC DDF Timing Relative To From Value Set Terminology [NCIt concept]
- CDISC DDF Timing Type Value Set Terminology [NCIt concept]
- CDISC DDF Transition Rule Attribute Terminology [NCIt concept]
- CDISC Protocol Study Arm Type Value Set Terminology [NCIt concept]
- CDISC SDTM Environmental Setting Terminology [NCIt concept]
- CDISC SDTM Epoch Terminology [NCIt concept]
- CDISC SDTM Intervention Model Terminology [NCIt concept]
- CDISC SDTM Mode of Subject Contact Terminology [NCIt concept]
- CDISC SDTM Sex of Study Group Terminology [NCIt concept]
- CDISC SDTM Study Type Terminology [NCIt concept]
- CDISC SDTM Trial Blinding Schema Terminology [NCIt concept]
- CDISC SDTM Trial Indication Type Terminology [NCIt concept]
- CDISC SDTM Trial Phase Terminology [NCIt concept]
- CDISC SDTM Trial Type Terminology [NCIt concept]
- Childcare Center [NCIt concept]
- City [NCIt concept]
- Clinic [NCIt concept]
- Clinical Encounter [NCIt concept]
- Clinical Encounter Description [NCIt concept]
- Clinical Encounter Name [NCIt concept]
- Clinical Encounter Type [NCIt concept]
- Clinical Study [NCIt concept]
- Clinical Study Activity Description [NCIt concept]
- Clinical Study Activity Name [NCIt concept]
- Clinical Study Sponsor [NCIt concept]
- Clinical Study by Intent [NCIt concept]
- Clinical Trial Epoch [NCIt concept]
- Clinical Trial Objective [NCIt concept]
- Code [NCIt concept]
- Code System Name [NCIt concept]
- Code Value [NCIt concept]
- Coding System Version [NCIt concept]
- Condition Assignments [NCIt concept]
- Contact Mode [NCIt concept]
- Continuation Therapy Epoch [NCIt concept]
- Control Arm [NCIt concept]
- Correctional Institution [NCIt concept]
- Country [NCIt concept]
- Crossover Study [NCIt concept]
- Cure Study [NCIt concept]
- Data Generated Within Study [NCIt concept]
- Decode Text [NCIt concept]
- Device Feasibility Study [NCIt concept]
- Device-Drug Interaction Study [NCIt concept]
- Diagnosis Study [NCIt concept]
- Disease Indication Code [NCIt concept]
- Disease Modifying Treatment Study [NCIt concept]
- District [NCIt concept]
- Dose Finding Study [NCIt concept]
- Dose Proportionality Study [NCIt concept]
- Dose Response Study [NCIt concept]
- Double Blind Study [NCIt concept]
- Draft [NCIt concept]
- Drug-Drug Interaction Study [NCIt concept]
- Efficacy Study [NCIt concept]
- Electrocardiographic Study [NCIt concept]
- End Point [NCIt concept]
- End to End [NCIt concept]
- End to Start [NCIt concept]
- Environmental Setting [NCIt concept]
- Epoch Description [NCIt concept]
- Epoch Name [NCIt concept]
- Estimand [NCIt concept]
- Expanded Access Study [NCIt concept]
- Exploratory Endpoint [NCIt concept]
- Factorial Study [NCIt concept]
- Farm [NCIt concept]
- Female [NCIt concept]
- Final [NCIt concept]
- Fixed Reference Timing Type [NCIt concept]
- Follow-Up Epoch [NCIt concept]
- Food Effect Study [NCIt concept]
- Group Sequential Design [NCIt concept]
- Health Services Research [NCIt concept]
- Healthcare Facility [NCIt concept]
- Historical Data [NCIt concept]
- Home [NCIt concept]
- Hospital [NCIt concept]
- Household Environment [NCIt concept]
- Identifier Provider Organization Name [NCIt concept]
- Immunogenicity Study [NCIt concept]
- In Person [NCIt concept]
- In the Field [NCIt concept]
- Induction Therapy Epoch [NCIt concept]
- Institution [NCIt concept]
- Interactive Voice Response System [NCIt concept]
- Intercurrent Event [NCIt concept]
- Intercurrent Event Description [NCIt concept]
- Intercurrent Event Name [NCIt concept]
- Intercurrent Event Strategy [NCIt concept]
- Intervention Description [NCIt concept]
- Intervention Model [NCIt concept]
- Interventional Study [NCIt concept]
- Investigational Arm [NCIt concept]
- Investigational Intervention Code [NCIt concept]
- Long-term Follow-up Epoch [NCIt concept]
- Lower Timing Window [NCIt concept]
- Main Timeline Indicator [NCIt concept]
- Male [NCIt concept]
- Motor Vehicle [NCIt concept]
- Next Clinical Encounter Identifier [NCIt concept]
- Next Epoch Identifier [NCIt concept]
- No Intervention Arm [NCIt concept]
- Non-household Environment [NCIt concept]
- Not Applicable [NCIt concept]
- Not In Clinic [NCIt concept]
- Observation Study Epoch [NCIt concept]
- Observational Study [NCIt concept]
- Observer Blind Study [NCIt concept]
- Obsolete [NCIt concept]
- Official Protocol Title [NCIt concept]
- Open Label Study [NCIt concept]
- Open Label Treatment Epoch [NCIt concept]
- Open Label for Treatment And Double Blind to Dose [NCIt concept]
- Organization Identifier [NCIt concept]
- Organization Name [NCIt concept]
- Organization Type [NCIt concept]
- Parallel Study [NCIt concept]
- Patient Registry Study [NCIt concept]
- Pending Review [NCIt concept]
- Pharmacodynamic Study [NCIt concept]
- Pharmacoeconomic Study [NCIt concept]
- Pharmacogenetic Study [NCIt concept]
- Pharmacogenomic Study [NCIt concept]
- Pharmacokinetic Study [NCIt concept]
- Phase 0 Trial [NCIt concept]
- Phase I Trial [NCIt concept]
- Phase I/II Trial [NCIt concept]
- Phase II Trial [NCIt concept]
- Phase II/III Trial [NCIt concept]
- Phase III Trial [NCIt concept]
- Phase IIIa Trial [NCIt concept]
- Phase IIIb Trial [NCIt concept]
- Phase IIa Trial [NCIt concept]
- Phase IIb Trial [NCIt concept]
- Phase IV Trial [NCIt concept]
- Phase V Trial [NCIt concept]
- Physical Medical Procedure [NCIt concept]
- Placebo Control Arm [NCIt concept]
- Planned Maximum Age of Subjects [NCIt concept]
- Planned Minimum Age of Subjects [NCIt concept]
- Planned Study Arm Name [NCIt concept]
- Planned Subject Number [NCIt concept]
- Population-Level Summary [NCIt concept]
- Position Effect Trial [NCIt concept]
- Postal Code [NCIt concept]
- Prevention Study [NCIt concept]
- Previous Clinical Encounter Identifier [NCIt concept]
- Previous Epoch Identifier [NCIt concept]
- Primary Endpoint [NCIt concept]
- Procedure Code [NCIt concept]
- Procedure Description [NCIt concept]
- Procedure Name [NCIt concept]
- Professional Organization or Group [NCIt concept]
- Protocol Agent [NCIt concept]
- Protocol Amendment [NCIt concept]
- Protocol Treatment Arm [NCIt concept]
- Reactogenicity Study [NCIt concept]
- Real-world Data [NCIt concept]
- Regulatory Agency [NCIt concept]
- Response Code [NCIt concept]
- Response Code Enabled Indicator [NCIt concept]
- Run-in Period [NCIt concept]
- Safety Study [NCIt concept]
- Schedule Sequence Number [NCIt concept]
- Schedule Timeline [NCIt concept]
- Schedule Timeline Description [NCIt concept]
- Schedule Timeline Entry Condition [NCIt concept]
- Schedule Timeline Exit [NCIt concept]
- Schedule Timeline Name [NCIt concept]
- Scheduled Activity Instance [NCIt concept]
- Scheduled Decision Instance [NCIt concept]
- Scheduled Instance [NCIt concept]
- Scheduled Instance Type [NCIt concept]
- School [NCIt concept]
- Scientific Protocol Title [NCIt concept]
- Screening Epoch [NCIt concept]
- Screening Study [NCIt concept]
- Secondary Endpoint [NCIt concept]
- Sex of Study Group [NCIt concept]
- Sham Comparator Arm [NCIt concept]
- Shelter [NCIt concept]
- Shipment Confirmed by Signature [NCIt concept]
- Single Blind Study [NCIt concept]
- Single Group Study [NCIt concept]
- Social Setting [NCIt concept]
- Start to End [NCIt concept]
- Start to Start [NCIt concept]
- State [NCIt concept]
- Street Address [NCIt concept]
- Study Activity [NCIt concept]
- Study Activity is Conditional Indicator [NCIt concept]
- Study Activity is Conditional Reason [NCIt concept]
- Study Activity is Optional Indicator [NCIt concept]
- Study Activity is Optional Reason [NCIt concept]
- Study Arm [NCIt concept]
- Study Arm Data Origin Description [NCIt concept]
- Study Arm Data Origin Type [NCIt concept]
- Study Arm Type [NCIt concept]
- Study Design [NCIt concept]
- Study Design Cell [NCIt concept]
- Study Design Description [NCIt concept]
- Study Design Element Description [NCIt concept]
- Study Design Element Name [NCIt concept]
- Study Design Name [NCIt concept]
- Study Design Rationale [NCIt concept]
- Study Endpoint Description [NCIt concept]
- Study Endpoint Level [NCIt concept]
- Study Endpoint Purpose Description [NCIt concept]
- Study Epoch Type [NCIt concept]
- Study Identifier [NCIt concept]
- Study Objective Description [NCIt concept]
- Study Objective Level [NCIt concept]
- Study Population Description [NCIt concept]
- Study Procedure Type [NCIt concept]
- Study Procedure is Conditional Indicator [NCIt concept]
- Study Procedure is Conditional Reason [NCIt concept]
- Study Procedure is Optional Indicator [NCIt concept]
- Study Procedure is Optional Reason [NCIt concept]
- Study Protocol Amendment Effective Date [NCIt concept]
- Study Protocol Document Version Public Title [NCIt concept]
- Study Protocol Status [NCIt concept]
- Study Protocol Version [NCIt concept]
- Study Protocol Version Acronym [NCIt concept]
- Study Protocol Version Purpose Statement [NCIt concept]
- Study Registry [NCIt concept]
- Study Type [NCIt concept]
- Study Version [NCIt concept]
- Supportive Care Study [NCIt concept]
- Swallowing Function Trial [NCIt concept]
- Synthetic Data [NCIt concept]
- Target Study Population [NCIt concept]
- Target Study Population for Analysis [NCIt concept]
- Target Study Population for Analysis Description [NCIt concept]
- Telephone Call [NCIt concept]
- Therapeutic Area [NCIt concept]
- Therapeutic Equivalency Study [NCIt concept]
- Thorough QT Study [NCIt concept]
- Timing [NCIt concept]
- Timing Description [NCIt concept]
- Timing Relative To From Name [NCIt concept]
- Timing Type [NCIt concept]
- Timing Value [NCIt concept]
- Tolerability Study [NCIt concept]
- Transition End Rule [NCIt concept]
- Transition Rule [NCIt concept]
- Transition Rule Description [NCIt concept]
- Transition Start Rule [NCIt concept]
- Treatment Epoch [NCIt concept]
- Treatment Study [NCIt concept]
- Trial Blinding Schema [NCIt concept]
- Trial Design Element [NCIt concept]
- Trial Indication [NCIt concept]
- Trial Phase [NCIt concept]
- Trial Primary Objective [NCIt concept]
- Trial Secondary Objective [NCIt concept]
- Trial Title [NCIt concept]
- Trial Type [NCIt concept]
- Upper Timing Window [NCIt concept]
- Usability Testing Study [NCIt concept]
- Variable of Interest for the Estimand [NCIt concept]
- Virtual Data [NCIt concept]
- Visit [NCIt concept]
- Washout Period [NCIt concept]
- Water Effect Trial [NCIt concept]
- Window [NCIt concept]
- Worksite [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients