ID
5028
Descripción
ODM derived from http://clinicaltrials.gov/show/NCT00882245
Link
http://clinicaltrials.gov/show/NCT00882245
Palabras clave
Versiones (2)
- 9/12/13 9/12/13 - Martin Dugas
- 16/4/14 16/4/14 - Julian Varghese
Subido en
16 de abril de 2014
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY 4.0
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Eligibility NCT00882245 Atopic Dermatitis
Eligibility
- StudyEvent: Eligibility
Descripción
Exclusion Criteria
Alias
- UMLS CUI 2011AA
- CL425201
Descripción
Subjects with current or recurrent disease (except AD) that could affect the site of application, the action, absorption or disposition of the investigational product, or clinical or laboratory assessments.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0521116
- SNOMED CT 2011_0131
- 15240007
- UMLS CUI 2011AA
- C0012634
- SNOMED CT 2011_0131
- 64572001
- UMLS CUI 2011AA
- C0277556
- SNOMED CT 2011_0131
- 58184002
- UMLS CUI 2011AA
- CL411789
- UMLS CUI 2011AA
- C0011615
- SNOMED CT 2011_0131
- 24079001
- MedDRA 14.1
- 10012438
- ICD-10-CM Version 2010
- L20.9
- UMLS CUI 2011AA
- C0392760
- SNOMED CT 2011_0131
- 247591002
- UMLS CUI 2011AA
- C0013230
- UMLS CUI 2011AA
- C0582103
- SNOMED CT 2011_0131
- 225886003
Descripción
Subjects who have medical or psychiatric condition or laboratory abnormality that may increase the risk associated with trial participation or investigational product administration or may interfere with the interpretation of trial results and, in the judgement of the investigator, would make the subject inappropriate for entry into this trial.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0815173
- UMLS CUI 2011AA
- C0438215
- SNOMED CT 2011_0131
- 165346000
- MedDRA 14.1
- 10023547
- UMLS CUI 2011AA
- C0035647
- SNOMED CT 2011_0131
- 30207005
- HL7 V3 2006_05
- RSK
- UMLS CUI 2011AA
- C2348568
- UMLS CUI 2011AA
- C0013230
- UMLS CUI 2011AA
- C1533734
- SNOMED CT 2011_0131
- 416118004
- UMLS CUI 2011AA
- C0521102
- SNOMED CT 2011_0131
- 78235001
- UMLS CUI 2011AA
- C0459471
- SNOMED CT 2011_0131
- 280452008
- LOINC Version 232
- MTHU003869
- UMLS CUI 2011AA
- C0683954
Descripción
Subjects with any skin tattoo, scar, cuts, bruises, or other skin damage, including excessive UV exposure, at the possible drug application sites which could impact the application of the test agent or confound the local assessments during this study.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0221258
- UMLS CUI 2011AA
- C2004491
- SNOMED CT 2011_0131
- 12402003
- ICD-10-CM Version 2010
- L90.5
- UMLS CUI 2011AA
- C0000925
- SNOMED CT 2011_0131
- 283396008
- UMLS CUI 2011AA
- C0009938
- SNOMED CT 2011_0131
- 125667009
- MedDRA 14.1
- 10050584
- ICD-10-CM Version 2010
- T14.8
- ICD-9-CM Version 2011
- 924.9
- CTCAE 1105E
- E11666
- UMLS CUI 2011AA
- C0205394
- SNOMED CT 2011_0131
- 74964007
- UMLS CUI 2011AA
- C0037284
- SNOMED CT 2011_0131
- 95324001
- MedDRA 14.1
- 10040882
- UMLS CUI 2011AA
- C2938993
- MedDRA 14.1
- 10070687
- UMLS CUI 2011AA
- C0013227
- UMLS CUI 2011AA
- C0229986
- SNOMED CT 2011_0131
- 39801007
Descripción
Subjects with clinically significant renal and liver parameters, as defined as > 1.5 x creatinine and 3 x AST ULN (upper limit of normal) respectively.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0750502
- SNOMED CT 2011_0131
- 386134007
- UMLS CUI 2011AA
- C0022646
- SNOMED CT 2011_0131
- 64033007
- LOINC Version 232
- MTHU002935
- UMLS CUI 2011AA
- C0023884
- SNOMED CT 2011_0131
- 10200004
- LOINC Version 232
- MTHU002039
- UMLS CUI 2011AA
- C0449381
- SNOMED CT 2011_0131
- 252116004
- UMLS CUI 2011AA
- C0010294
- SNOMED CT 2011_0131
- 15373003
- MedDRA 14.1
- 10011358
- LOINC Version 232
- 38483-4
- UMLS CUI 2011AA
- C0004002
- SNOMED CT 2011_0131
- 26091008
- LOINC Version 232
- MTHU004883
- UMLS CUI 2011AA
- C1519815
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T14.8 (ICD-10-CM Version 2010)
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MTHU002935 (LOINC Version 232)
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