ID

12453

Description

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

Keywords

  1. 11/12/15 11/12/15 -
  2. 11/12/15 11/12/15 - Julian Varghese
  3. 11/20/15 11/20/15 -
Uploaded on

November 20, 2015

DOI

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License

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)

Patienteninformationen
Description

Patienteninformationen

Zentrum
Description

Study site number

Data type

integer

Alias
UMLS CUI [1]
C2825164
Pat.-Nr.:
Description

Patient number

Data type

integer

Alias
UMLS CUI [1]
C1830427
Name des Patienten:
Description

Patient name

Data type

text

Alias
UMLS CUI [1]
C1299487
Date of informed consent
Description

Date of informed consent

Data type

date

Alias
UMLS CUI [1]
C2985782
Einschlusskriterien
Description

Einschlusskriterien

Vorliegen einer unterschriebenen Einverständniserklärung
Description

Existence of signed informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Ausschlusskriterien
Description

Ausschlusskriterien

Infektionen der Atemwege innerhalb der letzten 4 Wochen
Description

Respiratory tract infections within past 4 weeks

Data type

boolean

Alias
UMLS CUI [1]
C0035243
Teilnahme an Medikamentenstudie innerhalb der letzten 30 Tage
Description

Participation in investigational drug study within past 30 days

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0013230
Klinischer Hinweis auf eine Mukoviszidose
Description

Clinical evidence of cystic fibrosis

Data type

boolean

Alias
UMLS CUI [1]
C0010674
Gruppeneinteilung
Description

Gruppeneinteilung

Gruppeneinteilung
Description

grouping

Data type

text

Alias
UMLS CUI [1]
C1522242
Diagnose wenn Patient mit Malabsorption
Description

Diagnose wenn Patient mit Malabsorption

Data type

text

Alias
UMLS CUI [1]
C0011900
Demographie
Description

Demographie

Geburtsdatum:
Description

Date of birth

Data type

date

Alias
UMLS CUI [1]
C0421451
Geschlecht
Description

sex

Data type

integer

Alias
UMLS CUI [1]
C0150831
Körpergewicht
Description

body weight

Data type

float

Measurement units
  • kg
Alias
UMLS CUI [1]
C0005910
kg
Größe:
Description

height

Data type

float

Measurement units
  • cm
Alias
UMLS CUI [1]
C0005890
cm
Hämolysetest
Description

Hämolysetest

Datum Blutentnahme
Description

Date of venous blood sampling

Data type

datetime

Alias
UMLS CUI [1]
C0190979
Laboruntersuchung
Description

Laboratory Procedure Date

Data type

datetime

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0011008
Ergebnis
Description

Results of Lab Testing

Data type

text

Alias
UMLS CUI [1]
C2826772
Weitere Laborergebnisse
Description

Weitere Laborergebnisse

Erythrozyten
Description

Erythrocytes

Data type

float

Measurement units
  • /μL
Alias
UMLS CUI [1]
C0014792
/μL
Vitamin E
Description

vitamin e

Data type

float

Measurement units
  • mg/dl
Alias
UMLS CUI [1]
C1142098
mg/dl
Retikulozyten
Description

reticulocytes

Data type

float

Alias
UMLS CUI [1]
C0206161
Einheit Laborergebnis Retikulozyten
Description

unit used for testing reticulocytes

Data type

text

Alias
UMLS CUI [1,1]
C1519795
UMLS CUI [1,2]
C0206161
Zink
Description

zinc

Data type

float

Alias
UMLS CUI [1]
C0373748
Masseinheit Zink
Description

unit used for testing zinc

Data type

text

Alias
UMLS CUI [1,1]
C1519795
UMLS CUI [1,2]
C0373748
Begleitmedikation der letzten 4 Wochen
Description

Begleitmedikation der letzten 4 Wochen

Begleitmedikation der letzten 4 Wochen
Description

Concomitant medication past 4 weeks

Data type

boolean

Alias
UMLS CUI [1]
C2347852
wenn Begleitmedikation in den letzten 4 Wochen auftraten
Description

wenn Begleitmedikation in den letzten 4 Wochen auftraten

Data type

text

Alias
UMLS CUI [1]
C2347852
Datum
Description

Date

Data type

date

Alias
UMLS CUI [1]
C0011008
Unterschrift Prüfer
Description

Signature Investigator

Data type

text

Alias
UMLS CUI [1]
C2346576

Similar models

Controlled multicenter trial of hemolysis as diagnostic test for cystic fibrosis (HemCF)

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Patienteninformationen
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])
Item Group
Einschlusskriterien
Existence of signed informed consent
Item
Vorliegen einer unterschriebenen Einverständniserklärung
boolean
C0021430 (UMLS CUI [1])
Item Group
Ausschlusskriterien
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])
Clinical evidence of cystic fibrosis
Item
Klinischer Hinweis auf eine Mukoviszidose
boolean
C0010674 (UMLS CUI [1])
Item Group
Gruppeneinteilung
Item
Gruppeneinteilung
text
C1522242 (UMLS CUI [1])
Code List
Gruppeneinteilung
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])
Item Group
Demographie
Date of birth
Item
Geburtsdatum:
date
C0421451 (UMLS CUI [1])
Item
Geschlecht
integer
C0150831 (UMLS CUI [1])
Code List
Geschlecht
CL Item
 (1)
CL Item
 (2)
body weight
Item
Körpergewicht
float
C0005910 (UMLS CUI [1])
height
Item
Größe:
float
C0005890 (UMLS CUI [1])
Item Group
Hämolysetest
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])
Item
Ergebnis
text
C2826772 (UMLS CUI [1])
Code List
Ergebnis
CL Item
Gd3+ (Gd3+)
CL Item
Gd3+ + Zn2+ (Gd3+ + Zn2+)
CL Item
 (Control 75)
Item Group
Weitere Laborergebnisse
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])
Code List
Einheit Laborergebnis Retikulozyten
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])
Code List
Masseinheit Zink
CL Item
 (μg/dl)
CL Item
 (μmol/l)
Item Group
Begleitmedikation der letzten 4 Wochen
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])

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