age 18 Years to 65 Years
Item
age 18 Years to 65 Years
boolean
C0001779 (UMLS CUI 2011AA)
397669002 (SNOMED CT 2011_0131)
Male or female patients (aged 18-65 years) with a diagnosis of AD.
Item
Male or female patients (aged 18-65 years) with a diagnosis of AD.
boolean
C0024554 (UMLS CUI 2011AA)
248153007 (SNOMED CT 2011_0131)
M (HL7 V3 2006_05)
C0015780 (UMLS CUI 2011AA)
248152002 (SNOMED CT 2011_0131)
F (HL7 V3 2006_05)
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
C0011615 (UMLS CUI 2011AA)
24079001 (SNOMED CT 2011_0131)
10012438 (MedDRA 14.1)
L20.9 (ICD-10-CM Version 2010)
Female patients of child bearing potential must be using a medically acceptable form of contraception.
Item
Female patients of child bearing potential must be using a medically acceptable form of contraception.
boolean
C0015780 (UMLS CUI 2011AA)
248152002 (SNOMED CT 2011_0131)
F (HL7 V3 2006_05)
C1148523 (UMLS CUI 2011AA)
C0237399 (UMLS CUI 2011AA)
C0027552 (UMLS CUI 2011AA)
410525008 (SNOMED CT 2011_0131)
C0700589 (UMLS CUI 2011AA)
146680009 (SNOMED CT 2011_0131)
10010808 (MedDRA 14.1)
Patients who are able and willing to give signed informed consent.
Item
Patients who are able and willing to give signed informed consent.
boolean
C0021430 (UMLS CUI 2011AA)
Patients who have pruritus exceed the reference range.
Item
Patients who have pruritus exceed the reference range.
boolean
C0033774 (UMLS CUI 2011AA)
418363000 (SNOMED CT 2011_0131)
10037087 (MedDRA 14.1)
L29 (ICD-10-CM Version 2010)
698.9 (ICD-9-CM Version 2011)
E13686 (CTCAE 1105E)
CL384738 (UMLS CUI 2011AA)
CL415192 (UMLS CUI 2011AA)
Patients who have a history of allergy to hydrocortisone.
Item
Patients who have a history of allergy to hydrocortisone.
boolean
CL421546 (UMLS CUI 2011AA)
392521001 (SNOMED CT 2011_0131)
C0020517 (UMLS CUI 2011AA)
257550005 (SNOMED CT 2011_0131)
T78.40 (ICD-10-CM Version 2010)
C0020268 (UMLS CUI 2011AA)
396458002 (SNOMED CT 2011_0131)
MTHU035101 (LOINC Version 232)
Patients who have a history of relevant drug hypersensitivity.
Item
Patients who have a history of relevant drug hypersensitivity.
boolean
CL421546 (UMLS CUI 2011AA)
392521001 (SNOMED CT 2011_0131)
C2347946 (UMLS CUI 2011AA)
C0552536 (UMLS CUI 2011AA)
MTHU002637 (LOINC Version 232)
Patients who have a history of contact dermatitis induced by a topical steroid.
Item
Patients who have a history of contact dermatitis induced by a topical steroid.
boolean
CL421546 (UMLS CUI 2011AA)
392521001 (SNOMED CT 2011_0131)
C0011616 (UMLS CUI 2011AA)
40275004 (SNOMED CT 2011_0131)
10012442 (MedDRA 14.1)
L25.9 (ICD-10-CM Version 2010)
C0205263 (UMLS CUI 2011AA)
16404004 (SNOMED CT 2011_0131)
C1522168 (UMLS CUI 2011AA)
6064005 (SNOMED CT 2011_0131)
TOPICAL (HL7 V3 2006_05)
C0038317 (UMLS CUI 2011AA)
116566001 (SNOMED CT 2011_0131)
Patients who are taking, and who are unwilling not to take, any medications or therapy prohibited by the protocol for the complete duration of the study.
Item
Patients who are taking, and who are unwilling not to take, any medications or therapy prohibited by the protocol for the complete duration of the study.
boolean
C2348563 (UMLS CUI 2011AA)
C1554075 (UMLS CUI 2011AA)
C0013227 (UMLS CUI 2011AA)
C0039798 (UMLS CUI 2011AA)
Patients who have a history or presence of any cancer.
Item
Malignant Neoplasms
boolean
C0006826 (UMLS CUI 2011AA)
363346000 (SNOMED CT 2011_0131)
10028997 (MedDRA 14.1)
MTHU010328 (LOINC Version 232)
C00-C96 (ICD-10-CM Version 2010)
Patients who have any renal or liver insufficiency, or clinically significant cardiac, renal or hepatic disease.
Item
Patients who have any renal or liver insufficiency, or clinically significant cardiac, renal or hepatic disease.
boolean
C1565489 (UMLS CUI 2011AA)
10038474 (MedDRA 14.1)
C1306571 (UMLS CUI 2011AA)
59927004 (SNOMED CT 2011_0131)
10056542 (MedDRA 14.1)
C0018799 (UMLS CUI 2011AA)
56265001 (SNOMED CT 2011_0131)
10061024 (MedDRA 14.1)
C0022658 (UMLS CUI 2011AA)
90708001 (SNOMED CT 2011_0131)
10029151 (MedDRA 14.1)
N18.9 (ICD-10-CM Version 2010)
C0023895 (UMLS CUI 2011AA)
235856003 (SNOMED CT 2011_0131)
10024670 (MedDRA 14.1)
K76.9 (ICD-10-CM Version 2010)
573.9 (ICD-9-CM Version 2011)
Patients who, in the opinion of the investigator, are not deemed eligible as determined by medical history, physical examination or clinical laboratory safety tests.
Item
Patients who, in the opinion of the investigator, are not deemed eligible as determined by medical history, physical examination or clinical laboratory safety tests.
boolean
C1518422 (UMLS CUI 2011AA)
C1302261 (UMLS CUI 2011AA)
399223003 (SNOMED CT 2011_0131)
C0521095 (UMLS CUI 2011AA)
436000 (SNOMED CT 2011_0131)
C0262926 (UMLS CUI 2011AA)
417662000 (SNOMED CT 2011_0131)
MTHU027722 (LOINC Version 232)
C0031809 (UMLS CUI 2011AA)
5880005 (SNOMED CT 2011_0131)
10034986 (MedDRA 14.1)
MTHU028014 (LOINC Version 232)
89.7 (ICD-9-CM Version 2011)
C0036043 (UMLS CUI 2011AA)
C0022885 (UMLS CUI 2011AA)
15220000 (SNOMED CT 2011_0131)
10059938 (MedDRA 14.1)
Patients who have pruritus associated with conditions other than AD.
Item
Patients who have pruritus associated with conditions other than AD.
boolean
C0033774 (UMLS CUI 2011AA)
418363000 (SNOMED CT 2011_0131)
10037087 (MedDRA 14.1)
L29 (ICD-10-CM Version 2010)
698.9 (ICD-9-CM Version 2011)
E13686 (CTCAE 1105E)
C0332281 (UMLS CUI 2011AA)
47429007 (SNOMED CT 2011_0131)
C0348080 (UMLS CUI 2011AA)
260905004 (SNOMED CT 2011_0131)
COND (HL7 V3 2006_05)
CL411789 (UMLS CUI 2011AA)
C0011615 (UMLS CUI 2011AA)
24079001 (SNOMED CT 2011_0131)
10012438 (MedDRA 14.1)
L20.9 (ICD-10-CM Version 2010)
Patients who have pruritus only on the face and head.
Item
Patients who have pruritus only on the face and head.
boolean
C0033774 (UMLS CUI 2011AA)
418363000 (SNOMED CT 2011_0131)
10037087 (MedDRA 14.1)
L29 (ICD-10-CM Version 2010)
698.9 (ICD-9-CM Version 2011)
E13686 (CTCAE 1105E)
C0205171 (UMLS CUI 2011AA)
50607009 (SNOMED CT 2011_0131)
C0015450 (UMLS CUI 2011AA)
89545001 (SNOMED CT 2011_0131)
MTHU003030 (LOINC Version 232)
C0018670 (UMLS CUI 2011AA)
69536005 (SNOMED CT 2011_0131)
MTHU001435 (LOINC Version 232)
Patients who, in the opinion of the investigator, have clinically relevant history or presence of any disease, or surgical history other than AD which is likely to affect the conduct of the study.
Item
Patients who, in the opinion of the investigator, have clinically relevant history or presence of any disease, or surgical history other than AD which is likely to affect the conduct of the study.
boolean
C0012634 (UMLS CUI 2011AA)
64572001 (SNOMED CT 2011_0131)
C0455610 (UMLS CUI 2011AA)
161615003 (SNOMED CT 2011_0131)
CL411789 (UMLS CUI 2011AA)
C0011615 (UMLS CUI 2011AA)
24079001 (SNOMED CT 2011_0131)
10012438 (MedDRA 14.1)
L20.9 (ICD-10-CM Version 2010)
C0392760 (UMLS CUI 2011AA)
247591002 (SNOMED CT 2011_0131)
C0681872 (UMLS CUI 2011AA)
Patients who have used M5161(active ingredient of M516102).
Item
Patients who have used M5161(active ingredient of M516102).
boolean
C1524063 (UMLS CUI 2011AA)
260676000 (SNOMED CT 2011_0131)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C0439861 (UMLS CUI 2011AA)
105590001 (SNOMED CT 2011_0131)
C1372955 (UMLS CUI 2011AA)
C0304229 (UMLS CUI 2011AA)
902003 (SNOMED CT 2011_0131)
Patients who cannot communicate reliably with the investigator.
Item
Patients who cannot communicate reliably with the investigator.
boolean
C1299582 (UMLS CUI 2011AA)
371151008 (SNOMED CT 2011_0131)
C1272703 (UMLS CUI 2011AA)
385669000 (SNOMED CT 2011_0131)
C0009452 (UMLS CUI 2011AA)
263536004 (SNOMED CT 2011_0131)
MTHU021752 (LOINC Version 232)
CL102947 (UMLS CUI 2011AA)
Patients who are pregnant or lactating.
Item
Patients who are pregnant or lactating.
boolean
C0549206 (UMLS CUI 2011AA)
10036586 (MedDRA 14.1)
C2828358 (UMLS CUI 2011AA)
Patients who have used any IMP and/or participated in any clinical trial within 3 months.
Item
Patients who have used any IMP and/or participated in any clinical trial within 3 months.
boolean
C1524063 (UMLS CUI 2011AA)
260676000 (SNOMED CT 2011_0131)
C0162537 (UMLS CUI 2011AA)
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
C0205394 (UMLS CUI 2011AA)
74964007 (SNOMED CT 2011_0131)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)