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documentation:next_cdm:clinical_trial [2017/01/13 18:05]
vojtechhuser
documentation:next_cdm:clinical_trial [2017/01/13 18:07] (current)
vojtechhuser
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 ===== Understanding Role / Relevance of Clinical Trial Data in the CDM===== ===== Understanding Role / Relevance of Clinical Trial Data in the CDM=====
  
-Proposing person: Vojtech Huser (and possibly others)+Proposing person: Vojtech Huser (someone initially posted this to the wiki (not indicating the source), I got assigned to it
  
-Forum thread:​http://​forums.ohdsi.org/​t/​omop-cdm-and-clinical-trials/​2109+Forum thread: http://​forums.ohdsi.org/​t/​omop-cdm-and-clinical-trials/​2109
  
-**Use Case:**+ 
 +**Use Case(s):**
  1. observational trial collects CRF data but also wants to digest any EHR updates (e.g., AllOfUs project)  1. observational trial collects CRF data but also wants to digest any EHR updates (e.g., AllOfUs project)
  
Line 17: Line 18:
 **Possible problems:** **Possible problems:**
  
- 1. convention for: person_id is in trial identified by NCT0000123456 and consented on date XYZ+ 1. convention for: person_id is in trial identified by NCT0000123456 and consented on date 
 + 
 + 2. convention for: CRF data is mapped to concepts. And concepts dictate where it goes. E.g., hematocrit CRF question goes into MEASUREMENT;​ others go into OBSERVATION.
  
- 2convention for: CRF data is mapped ​to concepts. And concepts dictate where it goes. E.g.hematocrit question goes into MEASUREMENT others go into observation+ 3if CRF question does not map to any conceptwhat do we do?
  
  3. convert OMOP CDM <Dx data> into SDTM  3. convert OMOP CDM <Dx data> into SDTM
documentation/next_cdm/clinical_trial.txt · Last modified: 2017/01/13 18:07 by vojtechhuser