ID

40184

Beskrivning

https://www.hl7.org/fhir/resourcelist.html (accessed at 26.01.2020) This form contains an incomplete implementation of the FHIR Resource Research Subject (1). After preliminary review, it contains the data elements that request clinical information.

Länk

https://www.hl7.org/fhir/resourcelist.html

Nyckelord

Versioner (3)
  1. 2020-02-24 2020-02-24 -
  2. 2020-03-05 2020-03-05 -
  3. 2020-03-18 2020-03-18 -
Rättsinnehavare

HL7 FHIR

Uppladdad den

18 mars 2020

DOI

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Licens

Creative Commons BY-NC 4.0
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FHIR v4.0.1

Engelsk

Resource Research Subject (1)

1 Formulär  
ResearchSubject
Beskrivning

ResearchSubject

Alias
UMLS CUI-1
C0080105
ResearchSubject.status
Beskrivning

The current state of the subject. This element is labeled as a modifier because it is a status element that contains status entered-in-error which means that the resource should not be treated as valid.

Datatyp

text

Alias
UMLS CUI [1,1]
C0080105
UMLS CUI [1,2]
C0449438
ResearchSubject.period
Beskrivning

The dates the subject began and ended their participation in the study.

Datatyp

durationDatetime

Alias
UMLS CUI [1,1]
C0080105
UMLS CUI [1,2]
C0808070
UMLS CUI [1,3]
C0679823
UMLS CUI [2,1]
C0080105
UMLS CUI [2,2]
C0679823
UMLS CUI [2,3]
C0806020
UMLS CUI [3,1]
C0080105
UMLS CUI [3,2]
C0679823
UMLS CUI [3,3]
C0449238
ResearchSubject.study
Beskrivning

Reference to the study the subject is participating in.

Datatyp

text

Alias
UMLS CUI [1,1]
C0080105
UMLS CUI [1,2]
C1706462
UMLS CUI [1,3]
C0008972
UMLS CUI [1,4]
C0679823
ResearchSubject.assignedArm
Beskrivning

The name of the arm in the study the subject is expected to follow as part of this study.

Datatyp

text

Alias
UMLS CUI [1,1]
C0080105
UMLS CUI [1,2]
C1522541
UMLS CUI [1,3]
C0027365
UMLS CUI [1,4]
C1516050
ResearchSubject.actualArm
Beskrivning

The name of the arm in the study the subject actually followed as part of this study.

Datatyp

text

Alias
UMLS CUI [1,1]
C0080105
UMLS CUI [1,2]
C1522541
UMLS CUI [1,3]
C3900116
ResearchSubject.consent
Beskrivning

A record of the patient's informed agreement to participate in the study.

Datatyp

text

Alias
UMLS CUI [1,1]
C0080105
UMLS CUI [1,2]
C0021430
UMLS CUI [1,3]
C2355580
Tillbaka till toppen

Similar models

Resource Research Subject (1)

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
ResearchSubject
C0080105 (UMLS CUI-1)
ResearchSubject.status
Item
ResearchSubject.status
text
C0080105 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
ResearchSubject.period
Item
ResearchSubject.period
durationDatetime
C0080105 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
C0679823 (UMLS CUI [1,3])
C0080105 (UMLS CUI [2,1])
C0679823 (UMLS CUI [2,2])
C0806020 (UMLS CUI [2,3])
C0080105 (UMLS CUI [3,1])
C0679823 (UMLS CUI [3,2])
C0449238 (UMLS CUI [3,3])
ResearchSubject.study
Item
ResearchSubject.study
text
C0080105 (UMLS CUI [1,1])
C1706462 (UMLS CUI [1,2])
C0008972 (UMLS CUI [1,3])
C0679823 (UMLS CUI [1,4])
ResearchSubject.assignedArm
Item
ResearchSubject.assignedArm
text
C0080105 (UMLS CUI [1,1])
C1522541 (UMLS CUI [1,2])
C0027365 (UMLS CUI [1,3])
C1516050 (UMLS CUI [1,4])
ResearchSubject.actualArm
Item
ResearchSubject.actualArm
text
C0080105 (UMLS CUI [1,1])
C1522541 (UMLS CUI [1,2])
C3900116 (UMLS CUI [1,3])
ResearchSubject.consent
Item
ResearchSubject.consent
text
C0080105 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C2355580 (UMLS CUI [1,3])
Tillbaka till toppen 

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