ID

12627

Beschrijving

Evolution of Molecular Biomarkers in Acute Heart Failure Induced by Shock; ODM derived from: https://clinicaltrials.gov/show/NCT02141607

Link

https://clinicaltrials.gov/show/NCT02141607

Trefwoorden

  1. 07-12-15 07-12-15 -
Geüploaded op

7 december 2015

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Acute Heart Failure NCT02141607

Eligibility Acute Heart Failure NCT02141607

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
for patients in septic shock, severity: sofa score > 5
Beschrijving

patients in septic shock

Datatype

boolean

Alias
UMLS CUI [1]
C0036983
for patients in cardiogenic shock, severity: sofa score > 5
Beschrijving

patients in cardiogenic shock

Datatype

boolean

Alias
UMLS CUI [1]
C0036980
first blood sample available within 16 hours from admission to the icu.
Beschrijving

first blood sample available within 16 hours from admission to the icu

Datatype

boolean

Alias
UMLS CUI [1]
C1320532
only community medical acquired septic shock. we include patients with shock symptoms and shock diagnosis occurring within the first 48 hours from hospital admission
Beschrijving

community medical acquired septic shock

Datatype

boolean

Alias
UMLS CUI [1,1]
C0456394
UMLS CUI [1,2]
C0036983
informed consent available
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
risk of rapidly fatal illness and death within 24 hours
Beschrijving

risk of rapidly fatal illness and death within 24 hours

Datatype

boolean

Alias
UMLS CUI [1]
C2711184
UMLS CUI [2]
C1320532
patients already enrolled in other interventional studies
Beschrijving

Study subject participation status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
n > 4 units of red blood cells transfused
Beschrijving

n > 4 units of red blood cells transfused

Datatype

boolean

Alias
UMLS CUI [1]
C0199962
patients treated with plasma or whole blood
Beschrijving

patients treated with plasma or whole blood

Datatype

boolean

Alias
UMLS CUI [1]
C0278347
UMLS CUI [2]
C0005841
active hematological malignancy
Beschrijving

hematological malignancy

Datatype

boolean

Alias
UMLS CUI [1]
C0376545
metastatic cancer
Beschrijving

metastatic cancer

Datatype

boolean

Alias
UMLS CUI [1]
C0027627
immunodepression, including transplant patients: hiv+, constitutive immune system deficiency, immunosuppressive therapy, systemic corticosteroids (aerosols allowed)
Beschrijving

immunodepression, including transplant patients: hiv+, constitutive immune system deficiency, immunosuppressive therapy, systemic corticosteroids (aerosols allowed)

Datatype

boolean

Alias
UMLS CUI [1]
C1963758
UMLS CUI [2]
C0021051
UMLS CUI [3]
C0001175
patients with pre-existing end stage renal disease needing renal replacement therapy (rrt). the introduction of continuous veno-venous hemofiltration (cvvh), from the day of admission onward is allowed.
Beschrijving

patients with pre-existing end stage renal disease needing renal replacement therapy (rrt).

Datatype

boolean

Alias
UMLS CUI [1,1]
C0035078
UMLS CUI [1,2]
C0022671
cardiac surgery patients
Beschrijving

cardiac surgery

Datatype

boolean

Alias
UMLS CUI [1]
C0018821
cirrhosis child c
Beschrijving

cirrhosis child c

Datatype

boolean

Alias
UMLS CUI [1]
C3831115

Similar models

Eligibility Acute Heart Failure NCT02141607

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
patients in septic shock
Item
for patients in septic shock, severity: sofa score > 5
boolean
C0036983 (UMLS CUI [1])
patients in cardiogenic shock
Item
for patients in cardiogenic shock, severity: sofa score > 5
boolean
C0036980 (UMLS CUI [1])
first blood sample available within 16 hours from admission to the icu
Item
first blood sample available within 16 hours from admission to the icu.
boolean
C1320532 (UMLS CUI [1])
community medical acquired septic shock
Item
only community medical acquired septic shock. we include patients with shock symptoms and shock diagnosis occurring within the first 48 hours from hospital admission
boolean
C0456394 (UMLS CUI [1,1])
C0036983 (UMLS CUI [1,2])
informed consent
Item
informed consent available
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
risk of rapidly fatal illness and death within 24 hours
Item
risk of rapidly fatal illness and death within 24 hours
boolean
C2711184 (UMLS CUI [1])
C1320532 (UMLS CUI [2])
Study subject participation status
Item
patients already enrolled in other interventional studies
boolean
C2348568 (UMLS CUI [1])
n > 4 units of red blood cells transfused
Item
n > 4 units of red blood cells transfused
boolean
C0199962 (UMLS CUI [1])
patients treated with plasma or whole blood
Item
patients treated with plasma or whole blood
boolean
C0278347 (UMLS CUI [1])
C0005841 (UMLS CUI [2])
hematological malignancy
Item
active hematological malignancy
boolean
C0376545 (UMLS CUI [1])
metastatic cancer
Item
metastatic cancer
boolean
C0027627 (UMLS CUI [1])
immunodepression, including transplant patients: hiv+, constitutive immune system deficiency, immunosuppressive therapy, systemic corticosteroids (aerosols allowed)
Item
immunodepression, including transplant patients: hiv+, constitutive immune system deficiency, immunosuppressive therapy, systemic corticosteroids (aerosols allowed)
boolean
C1963758 (UMLS CUI [1])
C0021051 (UMLS CUI [2])
C0001175 (UMLS CUI [3])
patients with pre-existing end stage renal disease needing renal replacement therapy (rrt).
Item
patients with pre-existing end stage renal disease needing renal replacement therapy (rrt). the introduction of continuous veno-venous hemofiltration (cvvh), from the day of admission onward is allowed.
boolean
C0035078 (UMLS CUI [1,1])
C0022671 (UMLS CUI [1,2])
cardiac surgery
Item
cardiac surgery patients
boolean
C0018821 (UMLS CUI [1])
cirrhosis child c
Item
cirrhosis child c
boolean
C3831115 (UMLS CUI [1])

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