ID
43520
Description
ODM derived from http://clinicaltrials.gov/show/NCT00974740
Lien
http://clinicaltrials.gov/show/NCT00974740
Mots-clés
Versions (3)
- 07/12/2013 07/12/2013 - Martin Dugas
- 17/04/2014 17/04/2014 - Julian Varghese
- 20/09/2021 20/09/2021 -
Téléchargé le
20 septembre 2021
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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Eligibility NCT00974740 Type 1 Diabetes
Eligibility
- StudyEvent: Eligibility
Description
Ausschlusskriterien
Alias
- UMLS CUI 2011AA
- CL425201
Description
History of a malignancy
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0006826
Description
Presence of a clinically significant hepatic or renal disease, as indicated, but not limited to a serum creatinine elevated > ten percent above the upper limit of normal, elevation of AST or ALT > 3 times the upper limit of normal
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0023895
- SNOMED CT 2011_0131
- 235856003
- MedDRA 14.1
- 10024670
- ICD-10-CM Version 2010
- K76.9
- ICD-9-CM Version 2011
- 573.9
- UMLS CUI 2011AA
- C0022658
- SNOMED CT 2011_0131
- 90708001
- MedDRA 14.1
- 10029151
- ICD-10-CM Version 2010
- N18.9
- UMLS CUI 2011AA
- CL414623
- UMLS CUI 2011AA
- C0201976
- SNOMED CT 2011_0131
- 113075003
- MedDRA 14.1
- 10040230
- UMLS CUI 2011AA
- C0004002
- SNOMED CT 2011_0131
- 26091008
- LOINC Version 232
- MTHU004883
- UMLS CUI 2011AA
- C0001899
- SNOMED CT 2011_0131
- 56935002
- LOINC Version 232
- MTHU006766
- UMLS CUI 2011AA
- C1519815
Description
Any other acute or chronic condition that may affect the patient's response to treatment or might be associated with an increased risk for the patient to participate, as judged by the investigator
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0348080
- SNOMED CT 2011_0131
- 260905004
- HL7 V3 2006_05
- COND
- UMLS CUI 2011AA
- C0392760
- SNOMED CT 2011_0131
- 247591002
- UMLS CUI 2011AA
- C0521982
- SNOMED CT 2011_0131
- 182985004
- UMLS CUI 2011AA
- C0332281
- SNOMED CT 2011_0131
- 47429007
- UMLS CUI 2011AA
- C0205217
- HL7 V3 2006_05
- U
- UMLS CUI 2011AA
- C0679823
- HL7 V3 2006_05
- PART
- UMLS CUI 2011AA
- C0035647
- SNOMED CT 2011_0131
- 30207005
- HL7 V3 2006_05
- RSK
Description
Current use of anti-inflammatory or immunomodulatory drugs, antihypertensive, lipid-lowering, or antidiabetic drugs other than insulin
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C1524063
- SNOMED CT 2011_0131
- 260676000
- UMLS CUI 2011AA
- C0003211
- SNOMED CT 2011_0131
- 16403005, 372665008
- UMLS CUI 2011AA
- C0005525
- UMLS CUI 2011AA
- C0003364
- SNOMED CT 2011_0131
- 372586001
- UMLS CUI 2011AA
- C0086440
- SNOMED CT 2011_0131
- 57952007
- UMLS CUI 2011AA
- C0935929
- SNOMED CT 2011_0131
- 373245004
- UMLS CUI 2011AA
- CL411789
- UMLS CUI 2011AA
- C0021641
- SNOMED CT 2011_0131
- 67866001
- LOINC Version 232
- MTHU019392
Description
Pregnant or nursing women or women intending to become pregnant
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0043210
- SNOMED CT 2011_0131
- 224526002
- UMLS CUI 2011AA
- C0549206
- MedDRA 14.1
- 10036586
- UMLS CUI 2011AA
- C0006147
- MedDRA 14.1
- 10006247
- UMLS CUI 2011AA
- C0032992
- SNOMED CT 2011_0131
- 169565003
Description
Known or suspected allergy to atorvastatin or any component of the trial product
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0020517
- SNOMED CT 2011_0131
- 257550005
- ICD-10-CM Version 2010
- T78.40
- UMLS CUI 2011AA
- C0286651
- SNOMED CT 2011_0131
- 373444002
- UMLS CUI 2011AA
- C1705248
- UMLS CUI 2011AA
- C0304229
- SNOMED CT 2011_0131
- 902003
Description
Known myopathy, myalgia or myositis with a serum-CPK > 3 times the upper limit of normal
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0026848
- SNOMED CT 2011_0131
- 129565002
- MedDRA 14.1
- 10028641
- ICD-10-CM Version 2010
- G72.9
- ICD-9-CM Version 2011
- 359.9
- UMLS CUI 2011AA
- C0231528
- SNOMED CT 2011_0131
- 68962001
- MedDRA 14.1
- 10028323
- LOINC Version 232
- MTHU013523
- ICD-10-CM Version 2010
- M79.1
- CTCAE 1105E
- E12485
- UMLS CUI 2011AA
- C0027121
- SNOMED CT 2011_0131
- 26889001
- MedDRA 14.1
- 10028653
- ICD-10-CM Version 2010
- M60.9
- CTCAE 1105E
- E12489
- UMLS CUI 2011AA
- C0750860
- MedDRA 14.1
- 10040222
- UMLS CUI 2011AA
- C1519815
Description
Patients who had a severe blood loss (>= 400 mL, e.g. blood donation) within 2 months prior to visit 2
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0205082
- SNOMED CT 2011_0131
- 24484000
- UMLS CUI 2011AA
- CL353706
- UMLS CUI 2011AA
- C0005794
- SNOMED CT 2011_0131
- 25179006
Description
Any significant laboratory abnormality
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0750502
- SNOMED CT 2011_0131
- 386134007
- UMLS CUI 2011AA
- C0438215
- SNOMED CT 2011_0131
- 165346000
- MedDRA 14.1
- 10023547
Description
A serum LDL-cholesterol > 150 mg/dL at time of screening
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0428474
- SNOMED CT 2011_0131
- 166833005
- UMLS CUI 2011AA
- C0439547
- SNOMED CT 2011_0131
- 272105005
- UMLS CUI 2011AA
- C1409616
Description
Unwillingness to comply with study procedures
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0558080
- SNOMED CT 2011_0131
- 225465005
- UMLS CUI 2011AA
- C1321605
- SNOMED CT 2011_0131
- 405078008
- UMLS CUI 2011AA
- C0680734
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Eligibility
- StudyEvent: Eligibility
397669002 (SNOMED CT 2011_0131)
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64135003 (SNOMED CT 2011_0131)
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K76.9 (ICD-10-CM Version 2010)
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CL414623 (UMLS CUI 2011AA)
C0201976 (UMLS CUI 2011AA)
113075003 (SNOMED CT 2011_0131)
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C0004002 (UMLS CUI 2011AA)
26091008 (SNOMED CT 2011_0131)
MTHU004883 (LOINC Version 232)
C0001899 (UMLS CUI 2011AA)
56935002 (SNOMED CT 2011_0131)
MTHU006766 (LOINC Version 232)
C1519815 (UMLS CUI 2011AA)
260905004 (SNOMED CT 2011_0131)
COND (HL7 V3 2006_05)
C0392760 (UMLS CUI 2011AA)
247591002 (SNOMED CT 2011_0131)
C0521982 (UMLS CUI 2011AA)
182985004 (SNOMED CT 2011_0131)
C0332281 (UMLS CUI 2011AA)
47429007 (SNOMED CT 2011_0131)
C0205217 (UMLS CUI 2011AA)
U (HL7 V3 2006_05)
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
C0035647 (UMLS CUI 2011AA)
30207005 (SNOMED CT 2011_0131)
RSK (HL7 V3 2006_05)
260676000 (SNOMED CT 2011_0131)
C0003211 (UMLS CUI 2011AA)
16403005, 372665008 (SNOMED CT 2011_0131)
C0005525 (UMLS CUI 2011AA)
C0003364 (UMLS CUI 2011AA)
372586001 (SNOMED CT 2011_0131)
C0086440 (UMLS CUI 2011AA)
57952007 (SNOMED CT 2011_0131)
C0935929 (UMLS CUI 2011AA)
373245004 (SNOMED CT 2011_0131)
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10006247 (MedDRA 14.1)
C0032992 (UMLS CUI 2011AA)
169565003 (SNOMED CT 2011_0131)
257550005 (SNOMED CT 2011_0131)
T78.40 (ICD-10-CM Version 2010)
C0286651 (UMLS CUI 2011AA)
373444002 (SNOMED CT 2011_0131)
C1705248 (UMLS CUI 2011AA)
C0304229 (UMLS CUI 2011AA)
902003 (SNOMED CT 2011_0131)
129565002 (SNOMED CT 2011_0131)
10028641 (MedDRA 14.1)
G72.9 (ICD-10-CM Version 2010)
359.9 (ICD-9-CM Version 2011)
C0231528 (UMLS CUI 2011AA)
68962001 (SNOMED CT 2011_0131)
10028323 (MedDRA 14.1)
MTHU013523 (LOINC Version 232)
M79.1 (ICD-10-CM Version 2010)
E12485 (CTCAE 1105E)
C0027121 (UMLS CUI 2011AA)
26889001 (SNOMED CT 2011_0131)
10028653 (MedDRA 14.1)
M60.9 (ICD-10-CM Version 2010)
E12489 (CTCAE 1105E)
C0750860 (UMLS CUI 2011AA)
10040222 (MedDRA 14.1)
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24484000 (SNOMED CT 2011_0131)
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10023547 (MedDRA 14.1)
166833005 (SNOMED CT 2011_0131)
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272105005 (SNOMED CT 2011_0131)
C1409616 (UMLS CUI 2011AA)
225465005 (SNOMED CT 2011_0131)
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