ID
5058
Beschrijving
ODM derived from http://clinicaltrials.gov/show/NCT00974740
Link
http://clinicaltrials.gov/show/NCT00974740
Trefwoorden
Versies (3)
- 07-12-13 07-12-13 - Martin Dugas
- 17-04-14 17-04-14 - Julian Varghese
- 20-09-21 20-09-21 -
Geüploaded op
17 april 2014
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
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Eligibility NCT00974740 Type 1 Diabetes
Eligibility
- StudyEvent: Eligibility
Beschrijving
Ausschlusskriterien
Alias
- UMLS CUI 2011AA
- CL425201
Beschrijving
History of a malignancy
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0006826
Beschrijving
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
Datatype
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
Beschrijving
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
Datatype
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
Beschrijving
Current use of anti-inflammatory or immunomodulatory drugs, antihypertensive, lipid-lowering, or antidiabetic drugs other than insulin
Datatype
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
- C0003367
- 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
Beschrijving
Pregnant or nursing women or women intending to become pregnant
Datatype
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
Beschrijving
Known or suspected allergy to atorvastatin or any component of the trial product
Datatype
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
Beschrijving
Known myopathy, myalgia or myositis with a serum-CPK > 3 times the upper limit of normal
Datatype
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
Beschrijving
Patients who had a severe blood loss (>= 400 mL, e.g. blood donation) within 2 months prior to visit 2
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0205082
- SNOMED CT 2011_0131
- 24484000
- UMLS CUI 2011AA
- CL353706
- UMLS CUI 2011AA
- C0005794
- SNOMED CT 2011_0131
- 25179006
Beschrijving
Any significant laboratory abnormality
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0750502
- SNOMED CT 2011_0131
- 386134007
- UMLS CUI 2011AA
- C0438215
- SNOMED CT 2011_0131
- 165346000
- MedDRA 14.1
- 10023547
Beschrijving
A serum LDL-cholesterol > 150 mg/dL at time of screening
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0428474
- SNOMED CT 2011_0131
- 166833005
- UMLS CUI 2011AA
- C0439547
- SNOMED CT 2011_0131
- 272105005
- UMLS CUI 2011AA
- C1409616
Beschrijving
Unwillingness to comply with study procedures
Datatype
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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