ID
43514
Descripción
ODM derived from http://clinicaltrials.gov/show/NCT00980135
Link
http://clinicaltrials.gov/show/NCT00980135
Palabras clave
Versiones (2)
- 25/7/13 25/7/13 - Martin Dugas
- 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 NCT00980135 Atopic Dermatitis
Eligibility
- StudyEvent: Eligibility
Descripción
Ausschlusskriterien
Alias
- UMLS CUI 2011AA
- CL425201
Descripción
Any other skin disease at the test area that would interfere the clinical assessment in the opinion of the investigator
Tipo de datos
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
Descripción
Moles, tattoos, strong pigmentation, or scars at the test area that would interfere the clinical assessment
Tipo de datos
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
Descripción
Regular intake of antiphlogistic drugs (for example, NSAIDs)
Tipo de datos
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
Descripción
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)
Tipo de datos
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
Descripción
UV-therapy or the use of solarium within 30 days before screening as well as during the trial
Tipo de datos
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
Descripción
Any alternative treatment of AD (e.g. acupuncture, kinesiology, and homoeopathy) within 30 days before screening as well as during the trial
Tipo de datos
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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