Información:
Error:
ID
12453
Descripción
Controlled, multicenter trial of hemolysis as diagnostic test for cystic fibrosis (HemCF). Documentation part for control group. Principal Investigator PD Dr. Hermann Schillers, University Hospital of Muenster
Palabras clave
Versiones (3)
- 12/11/15 12/11/15 -
- 12/11/15 12/11/15 - Julian Varghese
- 20/11/15 20/11/15 -
Subido en
20 de noviembre de 2015
DOI
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Licencia
Creative Commons BY-NC 3.0
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Control group: Multicenter trial of hemolysis as diagnostic test for cystic fibrosis (HemCF)
Controlled multicenter trial of hemolysis as diagnostic test for cystic fibrosis (HemCF)
Similar models
Controlled multicenter trial of hemolysis as diagnostic test for cystic fibrosis (HemCF)
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Study site number
Item
Zentrum
integer
C2825164 (UMLS CUI [1])
Patient number
Item
Pat.-Nr.:
integer
C1830427 (UMLS CUI [1])
Patient name
Item
Name des Patienten:
text
C1299487 (UMLS CUI [1])
Date of informed consent
Item
date
C2985782 (UMLS CUI [1])
Existence of signed informed consent
Item
Vorliegen einer unterschriebenen Einverständniserklärung
boolean
C0021430 (UMLS CUI [1])
Respiratory tract infections within past 4 weeks
Item
Infektionen der Atemwege innerhalb der letzten 4 Wochen
boolean
C0035243 (UMLS CUI [1])
Participation in investigational drug study within past 30 days
Item
Teilnahme an Medikamentenstudie innerhalb der letzten 30 Tage
boolean
C2348568 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
Clinical evidence of cystic fibrosis
Item
Klinischer Hinweis auf eine Mukoviszidose
boolean
C0010674 (UMLS CUI [1])
CL Item
(Healthy individual with CFTR-mutation (delF508))
CL Item
(Healthy individual with CFTR-mutation (without delF508))
CL Item
(Healthy individual, related to CF-patient, without confirmed CFTR-mutation)
CL Item
(Healthy individual,without confirmed CFTR-mutation)
CL Item
(Patient with Malabsorption)
Diagnosis if malabsorption has been confirmed
Item
Diagnose wenn Patient mit Malabsorption
text
C0011900 (UMLS CUI [1])
Date of birth
Item
Geburtsdatum:
date
C0421451 (UMLS CUI [1])
CL Item
(1)
CL Item
(2)
body weight
Item
Körpergewicht
float
C0005910 (UMLS CUI [1])
height
Item
Größe:
float
C0005890 (UMLS CUI [1])
Date of venous blood sampling
Item
Datum Blutentnahme
datetime
C0190979 (UMLS CUI [1])
Laboratory Procedure Date
Item
Laboruntersuchung
datetime
C0022885 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
CL Item
Gd3+ (Gd3+)
CL Item
Gd3+ + Zn2+ (Gd3+ + Zn2+)
CL Item
(Control 75)
Erythrocytes
Item
Erythrozyten
float
C0014792 (UMLS CUI [1])
vitamin e
Item
Vitamin E
float
C1142098 (UMLS CUI [1])
reticulocytes
Item
Retikulozyten
float
C0206161 (UMLS CUI [1])
Item
Einheit Laborergebnis Retikulozyten
text
C1519795 (UMLS CUI [1,1])
C0206161 (UMLS CUI [1,2])
C0206161 (UMLS CUI [1,2])
CL Item
% (%)
CL Item
/nl (/nl)
zinc
Item
Zink
float
C0373748 (UMLS CUI [1])
Item
Masseinheit Zink
text
C1519795 (UMLS CUI [1,1])
C0373748 (UMLS CUI [1,2])
C0373748 (UMLS CUI [1,2])
CL Item
(μg/dl)
CL Item
(μmol/l)
Concomitant medication past 4 weeks
Item
Begleitmedikation der letzten 4 Wochen
boolean
C2347852 (UMLS CUI [1])
Specifiy concomitant medication
Item
wenn Begleitmedikation in den letzten 4 Wochen auftraten
text
C2347852 (UMLS CUI [1])
Date
Item
Datum
date
C0011008 (UMLS CUI [1])
Signature Investigator
Item
Unterschrift Prüfer
text
C2346576 (UMLS CUI [1])