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Study Data Tabulation Model Implementation Guide - W3

CDISC SDTM Implementation Guide (SDS Version ) CDISC, 2004. All rights reserved Page 1 Final July 14, 2004 Study Data Tabulation Model Implementation Guide : Human Clinical Trials Prepared by the CDISC Submission Data Standards Team Notes to Readers This is the approved Implementation Guide for Version 1 of the CDISC Study Data Tabulation Model This Implementation Guide comprises version of the Submission Data Standards. Revision History Date Version Summary of Changes 2004-06-25 Document Version Released version reflecting all changes identified during comment periods.

historical background on how to provide metadata descriptions for submission data. The primary goal of the Metadata Model is to provide regulatory reviewers with a clear understanding of the datasets provided in a submission by communicating clear descriptions of the structure, purpose, attributes, and contents of each dataset and dataset variable.

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Transcription of Study Data Tabulation Model Implementation Guide - W3

1 CDISC SDTM Implementation Guide (SDS Version ) CDISC, 2004. All rights reserved Page 1 Final July 14, 2004 Study Data Tabulation Model Implementation Guide : Human Clinical Trials Prepared by the CDISC Submission Data Standards Team Notes to Readers This is the approved Implementation Guide for Version 1 of the CDISC Study Data Tabulation Model This Implementation Guide comprises version of the Submission Data Standards. Revision History Date Version Summary of Changes 2004-06-25 Document Version Released version reflecting all changes identified during comment periods.

2 2004-07-14 Document Version Corrects minor typos and errors in sections , , , , , , CDISC SDTM Implementation Guide (SDS Version ) Page 2 CDISC, 2004. All rights reserved July 14, 2004 Final CONTENTS 1 ORGANIZATION OF THIS RELATIONSHIP TO PRIOR CDISC HOW TO READ THIS Implementation SUBMITTING 2 FUNDAMENTALS OF THE SDTM ..9 OBSERVATIONS AND DATA S E T S AND SPECIAL-PURPOSE 11 THE GENERAL DOMAIN 11 THE CDISC STANDARD DOMAIN CREATING A NEW How to Include Variables in New Domains (Steps 4 through 6).

3 15 3 SUBMITTING DATA IN STANDARD FORMAT ..16 STANDARD METADATA FOR DATASET CONTENTS AND USING THE CDISC DOMAIN MODELS IN REGULATORY CDISC Submission Dataset Definition Metadata ..17 CDISC Submission Value-Level Metadata ..19 4 ASSUMPTIONS FOR DOMAIN MODELS ..21 GENERAL ASSUMPTIONS FOR ALL General Dataset Assumptions ..21 General Variable Assumptions ..22 Coding and Controlled Terminology Assumptions.

4 23 Actual and Relative Time Assumptions ..25 Other Assumptions ..30 5 MODELS FOR SPECIAL PURPOSE DOMAINS ..35 Demographics Domain Model DM ..35 Assumptions for Demographics (DM) domain Model ..37 Comments Domain Model Assumptions for Comments (CM) domain Model ..39 6 DOMAIN MODELS BASED ON THE GENERAL CLASSES ..40 Concomitant Medications CM ..40 Assumptions for Concomitant Medications (CM) domain Model ..43 Exposure EX ..45 Assumptions for Exposure (EX) domain Model ..47 Substance Use - Assumptions for Substance Use (SU) domain Model .

5 51 Adverse Events AE ..53 Assumptions for Adverse Events (AE) domain Model ..57 Disposition DS ..59 Assumptions for Disposition (DS) domain Model ..60 CDISC SDTM Implementation Guide (SDS Version ) CDISC, 2004. All rights reserved Page 3 Final July 14, Medical History MH ..62 Assumptions for Medical History (MH) domain Model ..64 ECG Test Results EG ..66 Assumptions for ECG (EG) domain Model .

6 69 Inclusion/Exclusion Exceptions IE ..70 Assumptions for Inclusion/Exclusion Exceptions (IE) domain Model ..71 Laboratory Test Results Physical Examinations Assumptions for Physical Examinations (PE) domain Questionnaires Subject Characteristics SC ..82 Assumptions for Subject Characteristics (SC) domain Model ..83 Vital Signs VS ..84 7 TRIAL DESIGN PLANNED ELEMENTS, ARMS, AND Trial Elements ..88 Trial Arms ..89 Trial Visits.

7 90 SUBJECT ELEMENTS AND Subject Subject TRIAL Identifying Trial Developing the Trial Arms Table ..95 Distinguishing between Branches and Trial Epoch Concept ..101 Rules concept ..106 Recap of Trial Arms Variables ..106 Truncated Arms ..107 TRIAL Identifying Trial Elements ..109 Developing the Trial Elements Table .. 110 Recap of Trial Elements Variables.

8 112 Distinguishing Elements from Epochs .. 112 TRIAL 113 Identifying Trial Visits .. 113 Developing the Trial Visits Table .. 113 Recap of Trial Visits Variables .. 114 SUBJECT Identifying Subject Elements .. 115 Unplanned Elements .. 115 Deriving SE End Date/Times .. 115 Recap of Subject Elements 116 Using Subject Elements Data to Place Subject Data within an Element or Epoch .. 116 SUBJECT 116 Identifying Subject Visits .. 116 Recap of Subject Visits 117 TRIAL INCLUSION/EXCLUSION 117 HOW TO Model THE DESIGN OF A CLINICAL 118 CDISC SDTM Implementation Guide (SDS Version ) Page 4 CDISC, 2004.

9 All rights reserved July 14, 2004 Final 8 REPRESENTING RELATIONSHIPS AMONG DATASETS OR RECORDS .. 119 RELATING GROUPS OF RECORDS WITHIN A --GRPID RELATING PEER RECORDS IN SEPARATE RELREC DATA S E RELREC Dataset RELATING DEPENDENT RECORDS IN DIFFERENT RELREC Split Datasets Example ..123 RELATING NON-STANDARD VARIABLE VALUES TO A PARENT SUPPQUAL Dataset ..124 SUPPQUAL Examples ..125 Examples of how to use the SUPPQUAL dataset are listed in the table below.

10 125 Examples of data that should not be in the SUPPQUAL dataset include: ..126 RELATING COMMENTS TO A PARENT COMMENTS Example ..127 HOW TO DETERMINE WHERE DATA BELONG IN THE 9 Implementation EXAMPLES ..129 DEMOGRAPHICS EXAMPLE ..129 INTERVENTIONS EXAMPLES ..130 CM Example: Intermittent use of concomitant medications ..130 EX Examples: ..131 SU Examples:..134 EVENTS EXAMPLES ..140 AE Example: Mapping an AE CRF to CDISC AE.


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