ID
43401
Description
ODM derived from http://clinicaltrials.gov/show/NCT00669708
Link
http://clinicaltrials.gov/show/NCT00669708
Keywords
Versions (3)
- 12/9/13 12/9/13 - Martin Dugas
- 4/15/14 4/15/14 - Julian Varghese
- 9/20/21 9/20/21 -
Uploaded on
September 20, 2021
DOI
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License
Creative Commons BY 4.0
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Eligibility NCT00669708 Compensate the Roughness of the Skin
Eligibility
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI 2011AA
- CL425201
Description
pregnancy, lactating women
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0549206
- SNOMED CT 2011_0131
- 289908002
- MedDRA 14.1
- 10036556
- LOINC Version 232
- MTHU035048
- UMLS CUI 2011AA
- C2828358
- UMLS CUI 2011AA
- C0043210
- SNOMED CT 2011_0131
- 224526002
Description
drug abuse
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0013146
- SNOMED CT 2011_0131
- 26416006
- MedDRA 14.1
- 10013654
- LOINC Version 232
- LP36310-8
- ICD-9-CM Version 2011
- 305.90
Description
active psychosomatic and psychiatric disease
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0205177
- SNOMED CT 2011_0131
- 55561003
- UMLS CUI 2011AA
- C0033931
- SNOMED CT 2011_0131
- 37057007
- MedDRA 14.1
- 10049587
- ICD-10-CM Version 2010
- F45.9
- UMLS CUI 2011AA
- C0004936
- SNOMED CT 2011_0131
- 74732009
- MedDRA 14.1
- 10037174
- ICD-10-CM Version 2010
- F99
- ICD-9-CM Version 2011
- 290-319.99
Description
active cancer
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0006826
Description
topical application of tacrolimus, pimecrolimus, corticosteroids or capsaicin two weeks before study start
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0683174
- UMLS CUI 2011AA
- C0085149
- SNOMED CT 2011_0131
- 386975001
- LOINC Version 232
- MTHU001849
- UMLS CUI 2011AA
- C1099414
- SNOMED CT 2011_0131
- 385580005
- UMLS CUI 2011AA
- C0001617
- SNOMED CT 2011_0131
- 79440004
- UMLS CUI 2011AA
- C0006931
- SNOMED CT 2011_0131
- 95995002
- UMLS CUI 2011AA
- C0205448
- SNOMED CT 2011_0131
- 19338005
- UMLS CUI 2011AA
- C0439230
- SNOMED CT 2011_0131
- 258705008
- HL7 V3 2006_05
- WK
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C2348558
Description
intake of antihistamines, corticosteroids, cyclosporine A and other immunosuppressants, naltrexone, UV-therapy two weeks before study start
Data type
boolean
Alias
- UMLS CUI 2011AA
- C1512806
- UMLS CUI 2011AA
- C0019590
- SNOMED CT 2011_0131
- 372806008
- LOINC Version 232
- MTHU003328
- UMLS CUI 2011AA
- C0001617
- SNOMED CT 2011_0131
- 79440004
- UMLS CUI 2011AA
- C0010592
- SNOMED CT 2011_0131
- 387467008
- LOINC Version 232
- MTHU005140
- UMLS CUI 2011AA
- C0205394
- SNOMED CT 2011_0131
- 74964007
- UMLS CUI 2011AA
- C0021081
- SNOMED CT 2011_0131
- 372823004, 69431002
- UMLS CUI 2011AA
- C0027360
- SNOMED CT 2011_0131
- 373546002
- LOINC Version 232
- MTHU002303
- UMLS CUI 2011AA
- C0041626
- SNOMED CT 2011_0131
- 363695005
- MedDRA 14.1
- 10046850
- ICD-9-CM Version 2011
- 99.82
- UMLS CUI 2011AA
- C0205448
- SNOMED CT 2011_0131
- 19338005
- UMLS CUI 2011AA
- C0439230
- SNOMED CT 2011_0131
- 258705008
- HL7 V3 2006_05
- WK
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C2348558
Description
participation in any other research study during the previous 4 weeks
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0679823
- HL7 V3 2006_05
- PART
- UMLS CUI 2011AA
- C0205394
- SNOMED CT 2011_0131
- 74964007
- UMLS CUI 2011AA
- C0681814
- UMLS CUI 2011AA
- C0205156
- SNOMED CT 2011_0131
- 9130008
- UMLS CUI 2011AA
- C0205450
- SNOMED CT 2011_0131
- 9362000
- UMLS CUI 2011AA
- C0439230
- SNOMED CT 2011_0131
- 258705008
- HL7 V3 2006_05
- WK
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