ID

34651

Description

Can the Venus 1000 Help Clinicians Treat Patients With Severe Sepsis or Acute Heart Failure? The CVP Trial; ODM derived from: https://clinicaltrials.gov/show/NCT02258984

Link

https://clinicaltrials.gov/show/NCT02258984

Keywords

  1. 1/22/19 1/22/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

January 22, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Severe Sepsis NCT02258984

Eligibility Severe Sepsis NCT02258984

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age 18 years old or greater
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
english speaking
Description

Able to speak English Language

Data type

boolean

Alias
UMLS CUI [1,1]
C0564215
UMLS CUI [1,2]
C0376245
clinical diagnosis of: 1) severe sepsis, or 2) acute heart failure
Description

Severe Sepsis | Heart failure

Data type

boolean

Alias
UMLS CUI [1]
C1719672
UMLS CUI [2]
C0018801
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
traumatic injuries
Description

Traumatic injury

Data type

boolean

Alias
UMLS CUI [1]
C3263723
active bleeding
Description

Hemorrhage

Data type

boolean

Alias
UMLS CUI [1]
C0019080
pregnancy
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
prisoners
Description

Prisoners

Data type

boolean

Alias
UMLS CUI [1]
C0033167
central venous catheter placement in the internal jugular or subclavian veins
Description

Insertion of central venous catheter Internal jugular veins | Insertion of central venous catheter Subclavian veins

Data type

boolean

Alias
UMLS CUI [1,1]
C3521108
UMLS CUI [1,2]
C0226550
UMLS CUI [2,1]
C3521108
UMLS CUI [2,2]
C0038532
bilateral external jugular vein catheterizations
Description

Catheterization Bilateral External jugular veins

Data type

boolean

Alias
UMLS CUI [1,1]
C0007430
UMLS CUI [1,2]
C0238767
UMLS CUI [1,3]
C0226543
concurrent enrollment into an interventional clinical trial that may affect subject treatment
Description

Study Subject Participation Status | Interventional Study Affecting Therapeutic procedure

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C3274035
UMLS CUI [2,2]
C0392760
UMLS CUI [2,3]
C0087111

Similar models

Eligibility Severe Sepsis NCT02258984

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age 18 years old or greater
boolean
C0001779 (UMLS CUI [1])
Able to speak English Language
Item
english speaking
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
Severe Sepsis | Heart failure
Item
clinical diagnosis of: 1) severe sepsis, or 2) acute heart failure
boolean
C1719672 (UMLS CUI [1])
C0018801 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Traumatic injury
Item
traumatic injuries
boolean
C3263723 (UMLS CUI [1])
Hemorrhage
Item
active bleeding
boolean
C0019080 (UMLS CUI [1])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Prisoners
Item
prisoners
boolean
C0033167 (UMLS CUI [1])
Insertion of central venous catheter Internal jugular veins | Insertion of central venous catheter Subclavian veins
Item
central venous catheter placement in the internal jugular or subclavian veins
boolean
C3521108 (UMLS CUI [1,1])
C0226550 (UMLS CUI [1,2])
C3521108 (UMLS CUI [2,1])
C0038532 (UMLS CUI [2,2])
Catheterization Bilateral External jugular veins
Item
bilateral external jugular vein catheterizations
boolean
C0007430 (UMLS CUI [1,1])
C0238767 (UMLS CUI [1,2])
C0226543 (UMLS CUI [1,3])
Study Subject Participation Status | Interventional Study Affecting Therapeutic procedure
Item
concurrent enrollment into an interventional clinical trial that may affect subject treatment
boolean
C2348568 (UMLS CUI [1])
C3274035 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C0087111 (UMLS CUI [2,3])

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