ID

40279

Beschrijving

PCORnet Common Data Model (CDM) PCORNET Trial Patients who are enrolled in PCORnet clinical trials and PCORnet studies. PCORnet Common Data Model (CDM) The PCORnet Common Data Model (CDM) is a specification that defines a standard organization and representationof data for the PCORnet Distributed Research Network. The PCORnet CDM is a key component of the PCORnet Distributed Research Network (DRN) infrastructure.

Trefwoorden

Versies (3)
  1. 12-12-16 12-12-16 -
  2. 01-07-19 01-07-19 -
  3. 30-03-20 30-03-20 -
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PCORnet

Geüploaded op

30 maart 2020

DOI

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Licentie

Creative Commons BY-NC 4.0
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PCORnet Common Data Model (CDM) PCORNET

Engels

PCORNET Trial V4.1

1 Formulieren  
  1. StudyEvent: ODM
    1. PCORNET Trial V4.1
PCORNET Trial
Beschrijving

PCORNET Trial

Alias
UMLS CUI-1
C3871135
UMLS CUI-2
C0008976
Patient ID
Beschrijving

Arbitrary person-level identifier used to link across tables.

Datatype

text

Alias
UMLS CUI [1]
C2348585
Trial ID
Beschrijving

Each TRIALID is assigned by the PCORnet trial’s coordinating center.

Datatype

text

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C1300638
Participant ID
Beschrijving

Arbitrary person-level identifier used to uniquely identify a participant in a PCORnet trial. PARTICIPANTID is never repeated or reused for a specific clinical trial, and is generally assigned by trial-specific processes. It may be the same as a randomization ID.

Datatype

text

Alias
UMLS CUI [1]
C2348585
Trial Site ID
Beschrijving

Each TRIAL_SITEID is assigned by the PCORnet trial coordinating center.

Datatype

text

Alias
UMLS CUI [1,1]
C0450429
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C1300638
Trial Enroll Date
Beschrijving

Date on which the participant enrolled in the trial (generally coincides with trial consent process).

Datatype

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0679646
UMLS CUI [1,3]
C1516879
Trial End Date
Beschrijving

Date on which the participant completes participation in the trial.

Datatype

date

Alias
UMLS CUI [1,1]
C0679646
UMLS CUI [1,2]
C4283764
Trial Withdraw Date
Beschrijving

If applicable, date on which the participant withdraws consent from the trial.

Datatype

date

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C2349954
UMLS CUI [1,3]
C0011008
Trial Invite Code
Beschrijving

Textual strings used to uniquely identify invitations sent to potential participants, and allows acceptances to be associated back to the originating source. Where used, there should generally be a unique combination of PATID, TRIAL_NAME, and INVITE_CODE within each datamart. For example, this might include “co-enrollment ID strings” for e-mail invites or “verification codes” for letter invites.

Datatype

text

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C2826348
UMLS CUI [1,3]
C0805701
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Similar models

PCORNET Trial V4.1

1 Formulieren
  1. StudyEvent: ODM
    1. PCORNET Trial V4.1
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
PCORNET Trial
C3871135 (UMLS CUI-1)
C0008976 (UMLS CUI-2)
Patient ID
Item
Patient ID
text
C2348585 (UMLS CUI [1])
Trial ID
Item
Trial ID
text
C0008976 (UMLS CUI [1,1])
C1300638 (UMLS CUI [1,2])
Participant ID
Item
Participant ID
text
C2348585 (UMLS CUI [1])
Trial Site ID
Item
Trial Site ID
text
C0450429 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C1300638 (UMLS CUI [1,3])
Trial Enroll Date
Item
Trial Enroll Date
date
C0011008 (UMLS CUI [1,1])
C0679646 (UMLS CUI [1,2])
C1516879 (UMLS CUI [1,3])
Trial End Date
Item
Trial End Date
date
C0679646 (UMLS CUI [1,1])
C4283764 (UMLS CUI [1,2])
Trial Withdraw Date
Item
Trial Withdraw Date
date
C0008976 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Trial Invite Code
Item
Trial Invite Code
text
C0008976 (UMLS CUI [1,1])
C2826348 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
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