Informatie:
Fout:
ID
34651
Beschrijving
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
Trefwoorden
Versies (1)
- 22-01-19 22-01-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
22 januari 2019
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Severe Sepsis NCT02258984
Eligibility Severe Sepsis NCT02258984
- StudyEvent: Eligibility
Similar models
Eligibility Severe Sepsis NCT02258984
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
C0018801 (UMLS CUI [2])
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])
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])
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])
C3274035 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C0087111 (UMLS CUI [2,3])