ID
43998
Beschreibung
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
Stichworte
Versionen (2)
- 08.07.16 08.07.16 -
- 20.09.21 20.09.21 -
Hochgeladen am
20. September 2021
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY-NC-ND 3.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
SAE Form RICH study NCT02669589
SAE Form RICH study NCT02669589
- StudyEvent: ODM
Beschreibung
Seriousness criteria
Alias
- UMLS CUI-1
- C0871902
Beschreibung
Seriousness criteria
Datentyp
text
Alias
- UMLS CUI [1]
- C0871902
Beschreibung
Date of death
Datentyp
date
Alias
- UMLS CUI [1]
- C1148348
Beschreibung
Autopsy performed
Datentyp
text
Alias
- UMLS CUI [1]
- C0004398
Beschreibung
Cause of death
Datentyp
text
Alias
- UMLS CUI [1]
- C0007465
Beschreibung
Serious Adverse Event (SAE)
Alias
- UMLS CUI-1
- C1519255
Beschreibung
SAE: Diagnosis
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2919019
- UMLS CUI [1,2]
- C0011900
Beschreibung
Severity
Datentyp
text
Alias
- UMLS CUI [1]
- C0439793
Beschreibung
Onset date
Datentyp
date
Alias
- UMLS CUI [1]
- C0574845
Beschreibung
Adverse Event Outcome
Datentyp
text
Alias
- UMLS CUI [1]
- C1705586
Beschreibung
End date
Datentyp
date
Alias
- UMLS CUI [1]
- C0806020
Beschreibung
Reason for SAE
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0877248
Beschreibung
SAE: description
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0678257
Beschreibung
Treatment of SAE
Alias
- UMLS CUI-1
- C0087111
- UMLS CUI-2
- C0877248
Beschreibung
Drugs (Investigational drug/device - this is essential and mandatory information; Relevant concomitant medication - please do not enter any treatment of the SAE - Enter only drugs the patient started before the SAE)
Alias
- UMLS CUI-1
- C0013216
Beschreibung
Brand name
Datentyp
text
Alias
- UMLS CUI [1]
- C0592503
Beschreibung
Active substance
Datentyp
text
Alias
- UMLS CUI [1]
- C1254351
Beschreibung
Indication
Datentyp
text
Alias
- UMLS CUI [1]
- C3146298
Beschreibung
Causality
Datentyp
text
Alias
- UMLS CUI [1]
- C1547657
Beschreibung
Therapy duration
Datentyp
text
Alias
- UMLS CUI [1]
- C0444921
Beschreibung
Total daily dose and unit
Datentyp
text
Alias
- UMLS CUI [1]
- C2348070
- UMLS CUI [2]
- C1519795
Beschreibung
Route of administration
Datentyp
text
Alias
- UMLS CUI [1]
- C0013153
Beschreibung
Total absolute cumulative dose and unit
Datentyp
text
Alias
- UMLS CUI [1]
- C2986497
- UMLS CUI [2]
- C1519795
Beschreibung
Action SAE
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0441472
- UMLS CUI [1,2]
- C0877248
Beschreibung
Readministration
Datentyp
text
Alias
- UMLS CUI [1]
- C0376495
Beschreibung
Reaction to Readministration
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0376495
- UMLS CUI [1,2]
- C0443286
Beschreibung
Relevant Medical History - Information pertinent to understanding the case: e.g. underlying disease, pre-existing condition, concomitant/ intercurrent disease, surgery
Alias
- UMLS CUI-1
- C0262926
Beschreibung
Disease
Datentyp
text
Alias
- UMLS CUI [1]
- C0012634
Beschreibung
Start Date
Datentyp
date
Alias
- UMLS CUI [1]
- C0808070
Beschreibung
End Date
Datentyp
date
Alias
- UMLS CUI [1]
- C0806020
Beschreibung
Causality
Datentyp
text
Alias
- UMLS CUI [1]
- C1547657
Beschreibung
Relevant results of tests and procedures - attach results/ findings, if appropriate
Alias
- UMLS CUI-1
- C0392366
- UMLS CUI-2
- C0184661
Beschreibung
Tests and procedures
Datentyp
text
Alias
- UMLS CUI [1]
- C0392366
- UMLS CUI [2]
- C0184661
Beschreibung
Date
Datentyp
date
Alias
- UMLS CUI [1]
- C0011008
Beschreibung
Result
Datentyp
text
Alias
- UMLS CUI [1]
- C2826772
Beschreibung
Unit
Datentyp
text
Alias
- UMLS CUI [1]
- C1519795
Beschreibung
Normal range - lower limit
Datentyp
float
Alias
- UMLS CUI [1]
- C1518030
Beschreibung
Normal range - upper limit
Datentyp
float
Alias
- UMLS CUI [1]
- C1519815
Beschreibung
Comments
Alias
- UMLS CUI-1
- C0947611
Beschreibung
Investigator
Alias
- UMLS CUI-1
- C2826892
Beschreibung
Family name
Datentyp
text
Alias
- UMLS CUI [1]
- C1301584
Beschreibung
First name
Datentyp
text
Alias
- UMLS CUI [1]
- C1443235
Beschreibung
Institution address
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1301943
- UMLS CUI [1,2]
- C0376649
Beschreibung
Telephone
Datentyp
text
Alias
- UMLS CUI [1]
- C1515258
Beschreibung
Fax
Datentyp
text
Alias
- UMLS CUI [1]
- C1549619
Beschreibung
Datentyp
text
Alias
- UMLS CUI [1]
- C1705961
Beschreibung
Date of report
Datentyp
date
Alias
- UMLS CUI [1]
- C1302584
Beschreibung
Signature
Datentyp
text
Alias
- UMLS CUI [1]
- C1519316
Ähnliche Modelle
SAE Form RICH study NCT02669589
- StudyEvent: ODM
C0019994 (UMLS CUI [1,2])
C0011900 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,2])
C0678257 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
C1519795 (UMLS CUI [2])
C1519795 (UMLS CUI [2])
C0877248 (UMLS CUI [1,2])
C0443286 (UMLS CUI [1,2])
C0184661 (UMLS CUI-2)
C0184661 (UMLS CUI [2])
C0376649 (UMLS CUI [1,2])