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ID
12453
Beschrijving
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
Trefwoorden
Versies (3)
- 12-11-15 12-11-15 -
- 12-11-15 12-11-15 - Julian Varghese
- 20-11-15 20-11-15 -
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20 november 2015
DOI
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Licentie
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
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Study site number
Item
Study site number
integer
C2825164 (UMLS CUI [1])
Patient number
Item
Patient number
integer
C1830427 (UMLS CUI [1])
Patient name
Item
Patient name
text
C1299487 (UMLS CUI [1])
Date of informed consent
Item
Date of informed consent
date
C2985782 (UMLS CUI [1])
Existence of signed informed consent
Item
Existence of signed informed consent
boolean
C0021430 (UMLS CUI [1])
Respiratory tract infections within past 4 weeks
Item
Respiratory tract infections within past 4 weeks
boolean
C0035243 (UMLS CUI [1])
Participation in investigational drug study within past 30 days
Item
Participation in investigational drug study within past 30 days
boolean
C2348568 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
Clinical evidence of cystic fibrosis
Item
Clinical evidence of cystic fibrosis
boolean
C0010674 (UMLS CUI [1])
CL Item
Healthy individual with CFTR-mutation (delF508) (Healthy individual with CFTR-mutation (delF508))
CL Item
Healthy individual with CFTR-mutation (without delF508) (Healthy individual with CFTR-mutation (without delF508))
CL Item
Healthy individual, related to CF-patient, without confirmed CFTR-mutation (Healthy individual, related to CF-patient, without confirmed CFTR-mutation)
CL Item
Healthy individual,without confirmed CFTR-mutation (Healthy individual,without confirmed CFTR-mutation)
CL Item
Patient with Malabsorption (Patient with Malabsorption)
Diagnosis if malabsorption has been confirmed
Item
Diagnosis if malabsorption has been confirmed
text
C0011900 (UMLS CUI [1])
Date of birth
Item
Date of birth
date
C0421451 (UMLS CUI [1])
CL Item
male (1)
CL Item
female (2)
body weight
Item
Body weight
float
C0005910 (UMLS CUI [1])
height
Item
Height
float
C0005890 (UMLS CUI [1])
Date of venous blood sampling
Item
Date of venous blood sampling
datetime
C0190979 (UMLS CUI [1])
Laboratory Procedure Date
Item
Laboratory Procedure Date
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 (Control 75)
Erythrocytes
Item
Erythrocytes
float
C0014792 (UMLS CUI [1])
vitamin e
Item
Vitamin E
float
C1142098 (UMLS CUI [1])
reticulocytes
Item
reticulocytes
float
C0206161 (UMLS CUI [1])
Item
unit used for testing reticulocytes
text
C1519795 (UMLS CUI [1,1])
C0206161 (UMLS CUI [1,2])
C0206161 (UMLS CUI [1,2])
CL Item
% (%)
CL Item
/nl (/nl)
zinc
Item
Zinc
float
C0373748 (UMLS CUI [1])
Item
unit used for testing zinc
text
C1519795 (UMLS CUI [1,1])
C0373748 (UMLS CUI [1,2])
C0373748 (UMLS CUI [1,2])
CL Item
μg/dl (μg/dl)
CL Item
μmol/l (μmol/l)
Concomitant medication past 4 weeks
Item
Concomitant medication past 4 weeks
boolean
C2347852 (UMLS CUI [1])
Specifiy concomitant medication
Item
Specifiy concomitant medication
text
C2347852 (UMLS CUI [1])
Date
Item
Date
date
C0011008 (UMLS CUI [1])
Signature Investigator
Item
Signature Investigator
text
C2346576 (UMLS CUI [1])