ID
15701
Description
NCT02669589 EudraCT-Nr. 2014-004854-33 REGIONAL CITRATE VERSUS SYSTEMIC HEPARIN ANTICOAGULATION FOR CONTINUOUS RENAL REPLACEMENT THERAPY IN CRITICALLY ILL PATIENTS WITH ACUTE KIDNEY INJURY Study Chair: Alexander Zarbock, MD University Hospital Muenster
Keywords
Versions (1)
- 6/8/16 6/8/16 -
Uploaded on
June 8, 2016
DOI
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License
Creative Commons BY-NC-ND 3.0
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Eligibilitiy Criteria RICH Study NCT02669589
Eligibilitiy Criteria RICH Study NCT02669589
- StudyEvent: ODM
Description
Inclusion Criteria
Alias
- UMLS CUI-1
- C1512693
Description
Critical ill patients with acute kidney injury
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0010340
- UMLS CUI [1,2]
- C0022660
Description
Urinary excretion measurement
Data type
text
Alias
- UMLS CUI [1]
- C1285928
Description
Creatinine measurement
Data type
text
Alias
- UMLS CUI [1]
- C0201975
Description
Creatinine measurement specification
Data type
text
Alias
- UMLS CUI [1,1]
- C0201975
- UMLS CUI [1,2]
- C2348235
Description
Urea measurement
Data type
text
Alias
- UMLS CUI [1]
- C0523961
Description
Potassium measurement
Data type
text
Alias
- UMLS CUI [1]
- C0202194
Description
Magnesium measurement and anuria
Data type
text
Alias
- UMLS CUI [1]
- C0373675
- UMLS CUI [2]
- C0003460
Description
Blood pH measurement
Data type
text
Alias
- UMLS CUI [1]
- C0236489
Description
Urinary excretion measurement or anuria
Data type
text
Alias
- UMLS CUI [1]
- C1285928
- UMLS CUI [2]
- C0003460
Description
Oedema in organs resistant to diuretics
Data type
text
Alias
- UMLS CUI [1,1]
- C0013604
- UMLS CUI [1,2]
- C0332325
- UMLS CUI [1,3]
- C0013604
Description
Written informed consent
Alias
- UMLS CUI-1
- C0021430
Description
Written informed consent
Data type
text
Alias
- UMLS CUI [1]
- C0021430
Description
Date of informed consent
Data type
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0021430
Description
Time of informed consent
Data type
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0021430
Description
Therapy start
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0439659
Description
Exclusion Criteria - if one or more of the criteria is correct, exclude the patient
Alias
- UMLS CUI-1
- C0680251
Description
Bleeding risk
Data type
boolean
Alias
- UMLS CUI [1]
- C3251812
Description
Haemorrhagic diathesis
Data type
boolean
Alias
- UMLS CUI [1]
- C0019087
Description
Chronic Kidney Diseases
Data type
boolean
Alias
- UMLS CUI [1]
- C1561643
Description
Acute Kidney Injury requiring dialysis
Data type
boolean
Alias
- UMLS CUI [1]
- C2609414
- UMLS CUI [2]
- C0011946
Description
Chronic kidney failure requiring dialysis
Data type
boolean
Alias
- UMLS CUI [1]
- C0748304
Description
Anticoagluation therapy
Data type
boolean
Alias
- UMLS CUI [1]
- C0003281
Description
Hypersensitivity to anticoagulants or HIT
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0003280
- UMLS CUI [2]
- C0272285
Description
Acute Kidney Injury due to renal artery occlusion or surgical lesion of renal artery
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0553718
- UMLS CUI [1,2]
- C2609414
- UMLS CUI [2,1]
- C0282208
- UMLS CUI [2,2]
- C0035065
Description
Acute Kidney Injury
Data type
boolean
Alias
- UMLS CUI [1]
- C2609414
Description
DNR-Order
Data type
boolean
Alias
- UMLS CUI [1]
- C0582114
Description
Haemolytic uremic syndrome or thrombotic thrombocytopenic purpura
Data type
boolean
Alias
- UMLS CUI [1]
- C0019061
- UMLS CUI [2]
- C0034155
Description
Lactate acidosis
Data type
boolean
Alias
- UMLS CUI [1]
- C4039171
Description
Kidney transplantation
Data type
boolean
Alias
- UMLS CUI [1]
- C0022671
Description
Pregnancy test or breast feeding
Data type
boolean
Alias
- UMLS CUI [1]
- C0032976
- UMLS CUI [2]
- C0006147
Description
Abortus imminens
Data type
boolean
Alias
- UMLS CUI [1]
- C0948664
Description
Access to dialysis machines
Data type
boolean
Alias
- UMLS CUI [1,1]
- C3489407
- UMLS CUI [1,2]
- C0444454
Description
Study participation status
Data type
boolean
Alias
- UMLS CUI [1]
- C2348568
Description
Relation to study doctor
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0869014
- UMLS CUI [1,2]
- C0031831
Description
Living Arrangement - Institution
Data type
boolean
Alias
- UMLS CUI [1]
- C1546848
Description
Identification and Signature
Alias
- UMLS CUI-1
- C0205396
- UMLS CUI-2
- C1519316
Description
Date of report
Data type
date
Alias
- UMLS CUI [1]
- C1302584
Description
Time of report
Data type
time
Alias
- UMLS CUI [1]
- C1549507
Description
Doctor's name
Data type
text
Alias
- UMLS CUI [1,1]
- C0027365
- UMLS CUI [1,2]
- C0031831
Description
Doctor's signature
Data type
text
Alias
- UMLS CUI [1]
- C1519316
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Eligibilitiy Criteria RICH Study NCT02669589
- StudyEvent: ODM
C0019994 (UMLS CUI [1,2])
C0220908 (UMLS CUI [1,2])
C0220908 (UMLS CUI [1,2])
C0022660 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,2])
C0003460 (UMLS CUI [2])
C0003460 (UMLS CUI [2])
C0332325 (UMLS CUI [1,2])
C0013604 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,2])
C0011946 (UMLS CUI [2])
C0003280 (UMLS CUI [1,2])
C0272285 (UMLS CUI [2])
C2609414 (UMLS CUI [1,2])
C0282208 (UMLS CUI [2,1])
C0035065 (UMLS CUI [2,2])
C0034155 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
C0444454 (UMLS CUI [1,2])
C0031831 (UMLS CUI [1,2])
C1519316 (UMLS CUI-2)
C0031831 (UMLS CUI [1,2])
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