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

Mots-clés

  1. 12/11/2015 12/11/2015 -
  2. 12/11/2015 12/11/2015 - Julian Varghese
  3. 20/11/2015 20/11/2015 -
Téléchargé le

20 novembre 2015

DOI

Pour une demande vous connecter.

Licence

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)

Patient Identification
Description

Patient Identification

Study site number
Description

Study site number

Type de données

integer

Alias
UMLS CUI [1]
C2825164
Patient number
Description

Patient number

Type de données

integer

Alias
UMLS CUI [1]
C1830427
Patient name
Description

Patient name

Type de données

text

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

Date of informed consent

Type de données

date

Alias
UMLS CUI [1]
C2985782
Inclusion criteria
Description

Inclusion criteria

Existence of signed informed consent
Description

Existence of signed informed consent

Type de données

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

Type de données

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

Type de données

boolean

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

Clinical evidence of cystic fibrosis

Type de données

boolean

Alias
UMLS CUI [1]
C0010674
grouping
Description

grouping

Grouping
Description

grouping

Type de données

text

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

Diagnosis if malabsorption has been confirmed

Type de données

text

Alias
UMLS CUI [1]
C0011900
demography
Description

demography

Date of birth
Description

Date of birth

Type de données

date

Alias
UMLS CUI [1]
C0421451
Sex
Description

sex

Type de données

integer

Alias
UMLS CUI [1]
C0150831
Body weight
Description

body weight

Type de données

float

Unités de mesure
  • kg
Alias
UMLS CUI [1]
C0005910
kg
Height
Description

height

Type de données

float

Unités de mesure
  • cm
Alias
UMLS CUI [1]
C0005890
cm
hemolysis testing
Description

hemolysis testing

Date of venous blood sampling
Description

Date of venous blood sampling

Type de données

datetime

Alias
UMLS CUI [1]
C0190979
Laboratory Procedure Date
Description

Laboratory Procedure Date

Type de données

datetime

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

Results of Lab Testing

Type de données

text

Alias
UMLS CUI [1]
C2826772
Further laboratory results
Description

Further laboratory results

Erythrocytes
Description

Erythrocytes

Type de données

float

Unités de mesure
  • /μL
Alias
UMLS CUI [1]
C0014792
/μL
Vitamin E
Description

vitamin e

Type de données

float

Unités de mesure
  • mg/dl
Alias
UMLS CUI [1]
C1142098
mg/dl
reticulocytes
Description

reticulocytes

Type de données

float

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

unit used for testing reticulocytes

Type de données

text

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

zinc

Type de données

float

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

unit used for testing zinc

Type de données

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

Type de données

boolean

Alias
UMLS CUI [1]
C2347852
Specifiy concomitant medication
Description

Specifiy concomitant medication

Type de données

text

Alias
UMLS CUI [1]
C2347852
Date
Description

Date

Type de données

date

Alias
UMLS CUI [1]
C0011008
Signature Investigator
Description

Signature Investigator

Type de données

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)
Type de données
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])
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])
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])
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])
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])
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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