ID

4355

Description

ODM derived from http://clinicaltrials.gov/show/NCT00984867

Link

http://clinicaltrials.gov/show/NCT00984867

Keywords

Versions (2)
  1. 12/7/13 12/7/13 - Martin Dugas
  2. 4/17/14 4/17/14 - Julian Varghese
Uploaded on

December 7, 2013

DOI

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License

Creative Commons BY-NC 3.0 Legacy
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Eligibility NCT00984867 Type 2 Diabetes

German English

Eligibility

1 forms  
  1. StudyEvent: Eligibility
    1. Eligibility
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI 2011AA
CL425202
age at least 18 Years
Description

age at least 18 Years

Data type

boolean

Alias
UMLS CUI 2011AA
C0001779
SNOMED CT 2011_0131
397669002
Patients with type 2 diabetes
Description

Patients with type 2 diabetes

Data type

boolean

Alias
UMLS CUI 2011AA
C0011860
SNOMED CT 2011_0131
44054006
MedDRA 14.1
10012613
ICD-10-CM Version 2010
E08-E13
UMLS CUI 2011AA
C0011900
SNOMED CT 2011_0131
439401001
LOINC Version 232
MTHU008876
Patients who are not receiving treatment , or those who currently receive metformin, sitagliptin or vildagliptin or the combination of these
Description

Patients who are not receiving treatment , or those who currently receive metformin, sitagliptin or vildagliptin or the combination of these

Data type

boolean

Alias
UMLS CUI 2011AA
C1514756
UMLS CUI 2011AA
C1518422
UMLS CUI 2011AA
C0039798
UMLS CUI 2011AA
C1514756
UMLS CUI 2011AA
C0025598
SNOMED CT 2011_0131
372567009
LOINC Version 232
MTHU016062
UMLS CUI 2011AA
C1565750
SNOMED CT 2011_0131
423307000
UMLS CUI 2011AA
C1570906
SNOMED CT 2011_0131
428611002
UMLS CUI 2011AA
C1947911
Patients will be screened by a blood test and only those who need additional therapy can be enrolled
Description

Patients will be screened by a blood test and only those who need additional therapy can be enrolled

Data type

boolean

Alias
UMLS CUI 2011AA
C1409616
UMLS CUI 2011AA
C2121789
SNOMED CT 2011_0131
396550006
UMLS CUI 2011AA
C1516879
UMLS CUI 2011AA
C0205171
SNOMED CT 2011_0131
50607009
UMLS CUI 2011AA
C0030705
SNOMED CT 2011_0131
116154003
UMLS CUI 2011AA
C0686904
SNOMED CT 2011_0131
103325001
UMLS CUI 2011AA
C1706712
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI 2011AA
CL425201
Diabetes Mellitus, Insulin-Dependent
Description

Patients with type 1 diabetes

Data type

boolean

Alias
UMLS CUI 2011AA
C0011854
SNOMED CT 2011_0131
46635009
MedDRA 14.1
10067584
LOINC Version 232
MTHU020217
ICD-10-CM Version 2010
E10
Diabetes mellitus poor control
Description

Patients with very poorly controlled diabetes

Data type

boolean

Alias
UMLS CUI 2011AA
C0860161
MedDRA 14.1
10012619
Any clinically significant illness, which in the judgement of the investigator would compromise the patient's safety or successful participation in the clinical study
Description

Any clinically significant illness, which in the judgement of the investigator would compromise the patient's safety or successful participation in the clinical study

Data type

boolean

Alias
UMLS CUI 2011AA
C0221423
SNOMED CT 2011_0131
39104002
MedDRA 14.1
10040658
ICD-10-CM Version 2010
R69
UMLS CUI 2011AA
C0221099
SNOMED CT 2011_0131
260379002
UMLS CUI 2011AA
C1113679
UMLS CUI 2011AA
C1272703
SNOMED CT 2011_0131
385669000
UMLS CUI 2011AA
C0679823
HL7 V3 2006_05
PART
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008
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Similar models

Eligibility

1 forms
  1. StudyEvent: Eligibility
    1. Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion Criteria
CL425202 (UMLS CUI 2011AA)
age at least 18 Years
Item
age at least 18 Years
boolean
C0001779 (UMLS CUI 2011AA)
397669002 (SNOMED CT 2011_0131)
Patients with type 2 diabetes
Item
Patients with type 2 diabetes
boolean
C0011860 (UMLS CUI 2011AA)
44054006 (SNOMED CT 2011_0131)
10012613 (MedDRA 14.1)
E08-E13 (ICD-10-CM Version 2010)
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
Patients who are not receiving treatment , or those who currently receive metformin, sitagliptin or vildagliptin or the combination of these
Item
Patients who are not receiving treatment , or those who currently receive metformin, sitagliptin or vildagliptin or the combination of these
boolean
C1514756 (UMLS CUI 2011AA)
C1518422 (UMLS CUI 2011AA)
C0039798 (UMLS CUI 2011AA)
C1514756 (UMLS CUI 2011AA)
C0025598 (UMLS CUI 2011AA)
372567009 (SNOMED CT 2011_0131)
MTHU016062 (LOINC Version 232)
C1565750 (UMLS CUI 2011AA)
423307000 (SNOMED CT 2011_0131)
C1570906 (UMLS CUI 2011AA)
428611002 (SNOMED CT 2011_0131)
C1947911 (UMLS CUI 2011AA)
Patients will be screened by a blood test and only those who need additional therapy can be enrolled
Item
Patients will be screened by a blood test and only those who need additional therapy can be enrolled
boolean
C1409616 (UMLS CUI 2011AA)
C2121789 (UMLS CUI 2011AA)
396550006 (SNOMED CT 2011_0131)
C1516879 (UMLS CUI 2011AA)
C0205171 (UMLS CUI 2011AA)
50607009 (SNOMED CT 2011_0131)
C0030705 (UMLS CUI 2011AA)
116154003 (SNOMED CT 2011_0131)
C0686904 (UMLS CUI 2011AA)
103325001 (SNOMED CT 2011_0131)
C1706712 (UMLS CUI 2011AA)
Item Group
Exclusion Criteria
CL425201 (UMLS CUI 2011AA)
Patients with type 1 diabetes
Item
Diabetes Mellitus, Insulin-Dependent
boolean
C0011854 (UMLS CUI 2011AA)
46635009 (SNOMED CT 2011_0131)
10067584 (MedDRA 14.1)
MTHU020217 (LOINC Version 232)
E10 (ICD-10-CM Version 2010)
Patients with very poorly controlled diabetes
Item
Diabetes mellitus poor control
boolean
C0860161 (UMLS CUI 2011AA)
10012619 (MedDRA 14.1)
Any clinically significant illness, which in the judgement of the investigator would compromise the patient's safety or successful participation in the clinical study
Item
Any clinically significant illness, which in the judgement of the investigator would compromise the patient's safety or successful participation in the clinical study
boolean
C0221423 (UMLS CUI 2011AA)
39104002 (SNOMED CT 2011_0131)
10040658 (MedDRA 14.1)
R69 (ICD-10-CM Version 2010)
C0221099 (UMLS CUI 2011AA)
260379002 (SNOMED CT 2011_0131)
C1113679 (UMLS CUI 2011AA)
C1272703 (UMLS CUI 2011AA)
385669000 (SNOMED CT 2011_0131)
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
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