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

1 forms  
Patient Identification
Description

Patient Identification

Study site number
Description

Study site number

Data type

integer

Alias
UMLS CUI [1]
C2825164
Patient number
Description

Patient number

Data type

integer

Alias
UMLS CUI [1]
C1830427
Patient name
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
Inclusion criteria
Description

Inclusion criteria

Existence of signed informed consent
Description

Existence of signed informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
exclusion criteria
Description

exclusion criteria

Respiratory tract infections within past 4 weeks
Description

Respiratory tract infections within past 4 weeks

Data type

boolean

Alias
UMLS CUI [1]
C0035243
Participation in investigational drug study within past 30 days
Description

Participation in investigational drug study within past 30 days

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0013230
Clinical evidence of cystic fibrosis
Description

Clinical evidence of cystic fibrosis

Data type

boolean

Alias
UMLS CUI [1]
C0010674
grouping
Description

grouping

Grouping
Description

grouping

Data type

text

Alias
UMLS CUI [1]
C1522242
Diagnosis if malabsorption has been confirmed
Description

Diagnosis if malabsorption has been confirmed

Data type

text

Alias
UMLS CUI [1]
C0011900
demography
Description

demography

Date of birth
Description

Date of birth

Data type

date

Alias
UMLS CUI [1]
C0421451
Sex
Description

sex

Data type

integer

Alias
UMLS CUI [1]
C0150831
Body weight
Description

body weight

Data type

float

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

height

Data type

float

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

hemolysis testing

Date of venous blood sampling
Description

Date of venous blood sampling

Data type

datetime

Alias
UMLS CUI [1]
C0190979
Laboratory Procedure Date
Description

Laboratory Procedure Date

Data type

datetime

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0011008
Results of Lab Testing
Description

Results of Lab Testing

Data type

text

Alias
UMLS CUI [1]
C2826772
Further laboratory results
Description

Further laboratory results

Erythrocytes
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
reticulocytes
Description

reticulocytes

Data type

float

Alias
UMLS CUI [1]
C0206161
unit used for testing reticulocytes
Description

unit used for testing reticulocytes

Data type

text

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

zinc

Data type

float

Alias
UMLS CUI [1]
C0373748
unit used for testing zinc
Description

unit used for testing zinc

Data type

text

Alias
UMLS CUI [1,1]
C1519795
UMLS CUI [1,2]
C0373748
Concomitant medication past 4 weeks
Description

Concomitant medication past 4 weeks

Concomitant medication past 4 weeks
Description

Concomitant medication past 4 weeks

Data type

boolean

Alias
UMLS CUI [1]
C2347852
Specifiy concomitant medication
Description

Specifiy concomitant medication

Data type

text

Alias
UMLS CUI [1]
C2347852
Date
Description

Date

Data type

date

Alias
UMLS CUI [1]
C0011008
Signature Investigator
Description

Signature Investigator

Data type

text

Alias
UMLS CUI [1]
C2346576
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Similar models

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

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Patient Identification
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])
Clinical evidence of cystic fibrosis
Item
Clinical evidence of cystic fibrosis
boolean
C0010674 (UMLS CUI [1])
Item Group
grouping
Item
Grouping
text
C1522242 (UMLS CUI [1])
grouping
Code List
Grouping
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])
Item Group
demography
Date of birth
Item
Date of birth
date
C0421451 (UMLS CUI [1])
Item
Sex
integer
C0150831 (UMLS CUI [1])
sex
Code List
Sex
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])
Item Group
hemolysis testing
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])
Item
Results of Lab Testing
text
C2826772 (UMLS CUI [1])
Result
Code List
Results of Lab Testing
CL Item
Gd3+ (Gd3+)
CL Item
Gd3+ + Zn2+ (Gd3+ + Zn2+)
CL Item
Control 75 (Control 75)
Item Group
Further laboratory results
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])
unit Laboratory result reticulocytes
Code List
unit used for testing reticulocytes
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])
unit zinc
Code List
unit used for testing zinc
CL Item
μg/dl (μg/dl)
CL Item
μmol/l (μmol/l)
Item Group
Concomitant medication past 4 weeks
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])
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