ID
43520
Descripción
ODM derived from http://clinicaltrials.gov/show/NCT00974740
Link
http://clinicaltrials.gov/show/NCT00974740
Palabras clave
Versiones (3)
- 7/12/13 7/12/13 - Martin Dugas
- 17/4/14 17/4/14 - Julian Varghese
- 20/9/21 20/9/21 -
Subido en
20 de septiembre de 2021
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY 4.0
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Eligibility NCT00974740 Type 1 Diabetes
Eligibility
- StudyEvent: Eligibility
Descripción
Ausschlusskriterien
Alias
- UMLS CUI 2011AA
- CL425201
Descripción
History of a malignancy
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0006826
Descripción
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
Tipo de datos
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
Descripción
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
Tipo de datos
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
Descripción
Current use of anti-inflammatory or immunomodulatory drugs, antihypertensive, lipid-lowering, or antidiabetic drugs other than insulin
Tipo de datos
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
Descripción
Pregnant or nursing women or women intending to become pregnant
Tipo de datos
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
Descripción
Known or suspected allergy to atorvastatin or any component of the trial product
Tipo de datos
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
Descripción
Known myopathy, myalgia or myositis with a serum-CPK > 3 times the upper limit of normal
Tipo de datos
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
Descripción
Patients who had a severe blood loss (>= 400 mL, e.g. blood donation) within 2 months prior to visit 2
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0205082
- SNOMED CT 2011_0131
- 24484000
- UMLS CUI 2011AA
- CL353706
- UMLS CUI 2011AA
- C0005794
- SNOMED CT 2011_0131
- 25179006
Descripción
Any significant laboratory abnormality
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0750502
- SNOMED CT 2011_0131
- 386134007
- UMLS CUI 2011AA
- C0438215
- SNOMED CT 2011_0131
- 165346000
- MedDRA 14.1
- 10023547
Descripción
A serum LDL-cholesterol > 150 mg/dL at time of screening
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0428474
- SNOMED CT 2011_0131
- 166833005
- UMLS CUI 2011AA
- C0439547
- SNOMED CT 2011_0131
- 272105005
- UMLS CUI 2011AA
- C1409616
Descripción
Unwillingness to comply with study procedures
Tipo de datos
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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