ID
43514
Description
ODM derived from http://clinicaltrials.gov/show/NCT00980135
Link
http://clinicaltrials.gov/show/NCT00980135
Keywords
Versions (2)
- 7/25/13 7/25/13 - Martin Dugas
- 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 NCT00980135 Atopic Dermatitis
Eligibility
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI 2011AA
- CL425201
Description
Any other skin disease at the test area that would interfere the clinical assessment in the opinion of the investigator
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0205394
- SNOMED CT 2011_0131
- 74964007
- UMLS CUI 2011AA
- C0037274
- SNOMED CT 2011_0131
- 95320005
- MedDRA 14.1
- 10048768, 10040831
- LOINC Version 232
- MTHU031899
- UMLS CUI 2011AA
- C0392366
- SNOMED CT 2011_0131
- 272393004
- UMLS CUI 2011AA
- C0205146
- SNOMED CT 2011_0131
- 42798000
- LOINC Version 232
- MTHU009059
- UMLS CUI 2011AA
- C0521102
- SNOMED CT 2011_0131
- 78235001
- UMLS CUI 2011AA
- C0582103
- SNOMED CT 2011_0131
- 225886003
Description
Moles, tattoos, strong pigmentation, or scars at the test area that would interfere the clinical assessment
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0027960
- SNOMED CT 2011_0131
- 400010006
- MedDRA 14.1
- 10027806
- ICD-10-CM Version 2010
- D22
- UMLS CUI 2011AA
- C0221258
- UMLS CUI 2011AA
- C0442821
- SNOMED CT 2011_0131
- 260404005
- UMLS CUI 2011AA
- C0031911
- SNOMED CT 2011_0131
- 51083003
- MedDRA 14.1
- 10035018
- LOINC Version 232
- MTHU015062
- UMLS CUI 2011AA
- C2004491
- SNOMED CT 2011_0131
- 12402003
- ICD-10-CM Version 2010
- L90.5
- UMLS CUI 2011AA
- C0392366
- SNOMED CT 2011_0131
- 272393004
- UMLS CUI 2011AA
- C0205146
- SNOMED CT 2011_0131
- 42798000
- LOINC Version 232
- MTHU009059
Description
Regular intake of antiphlogistic drugs (for example, NSAIDs)
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0205272
- SNOMED CT 2011_0131
- 17854005
- UMLS CUI 2011AA
- C1512806
- UMLS CUI 2011AA
- C0003209
- SNOMED CT 2011_0131
- 330901000
- UMLS CUI 2011AA
- C0003211
- SNOMED CT 2011_0131
- 16403005, 372665008
Description
Any condition or treatment which might influence the trial (e.g. any treatment with topical antibiotics, antifungals, or corticoids) within 14 days prior to screening as well as during the trial (exception: topical treatment of AD lesions other than the test areas (for example, face) with low potency steroids restricted to small areas)
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0348080
- SNOMED CT 2011_0131
- 260905004
- HL7 V3 2006_05
- COND
- UMLS CUI 2011AA
- C0039798
- UMLS CUI 2011AA
- C0814606
- UMLS CUI 2011AA
- C0008976
- SNOMED CT 2011_0131
- 110465008
- UMLS CUI 2011AA
- C1522168
- SNOMED CT 2011_0131
- 6064005
- HL7 V3 2006_05
- TOPICAL
- UMLS CUI 2011AA
- C0003232
- SNOMED CT 2011_0131
- 255631004
- UMLS CUI 2011AA
- C0003308
- SNOMED CT 2011_0131
- 373219008
- UMLS CUI 2011AA
- C0001617
- SNOMED CT 2011_0131
- 79440004
Description
UV-therapy or the use of solarium within 30 days before screening as well as during the trial
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0041626
- SNOMED CT 2011_0131
- 363695005
- MedDRA 14.1
- 10046850
- ICD-9-CM Version 2011
- 99.82
- UMLS CUI 2011AA
- C1524063
- SNOMED CT 2011_0131
- 260676000
- UMLS CUI 2011AA
- C0183827
Description
Any alternative treatment of AD (e.g. acupuncture, kinesiology, and homoeopathy) within 30 days before screening as well as during the trial
Data type
boolean
Alias
- UMLS CUI 2011AA
- C1523987
- UMLS CUI 2011AA
- C0039798
- UMLS CUI 2011AA
- C0011615
- SNOMED CT 2011_0131
- 24079001
- MedDRA 14.1
- 10012438
- ICD-10-CM Version 2010
- L20.9
- UMLS CUI 2011AA
- C0394664
- SNOMED CT 2011_0131
- 44868003
- MedDRA 14.1
- 10000646
- UMLS CUI 2011AA
- C0282567
- UMLS CUI 2011AA
- C0684199
- SNOMED CT 2011_0131
- 182968001
- MedDRA 14.1
- 10020363
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