Eligibility NCT00420472 Kidney Transplantation

ODM derived from http://clinicaltrials.gov/show/NCT00420472

  1. StudyEvent: Eligibility
    1. Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Einschlusskriterien
CL425202 (UMLS CUI 2011AA)
age at least 18 Years
Item
Alter mindestens 18 Jahre
boolean
C0001779 (UMLS CUI 2011AA)
397669002 (SNOMED CT 2011_0131)
adult patients, >=18 years of age
Item
Erwachsener, erwachsen
boolean
C0001675 (UMLS CUI 2011AA)
133936004 (SNOMED CT 2011_0131)
first or second kidney transplant
Item
first or second kidney transplant
boolean
C0205435 (UMLS CUI 2011AA)
255216001 (SNOMED CT 2011_0131)
C0205436 (UMLS CUI 2011AA)
81170007 (SNOMED CT 2011_0131)
C0022671 (UMLS CUI 2011AA)
70536003 (SNOMED CT 2011_0131)
10038533 (MedDRA 14.1)
55.6 (ICD-9-CM Version 2011)
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
EC-MPS therapy for >=6 months, with a stable dose for >=2 months
Item
EC-MPS therapy for >=6 months, with a stable dose for >=2 months
boolean
C0039226 (UMLS CUI 2011AA)
385059007 (SNOMED CT 2011_0131)
ECTAB (HL7 V3 2006_05)
C1337395 (UMLS CUI 2011AA)
426216009 (SNOMED CT 2011_0131)
C0039798 (UMLS CUI 2011AA)
C0205452 (UMLS CUI 2011AA)
68244004 (SNOMED CT 2011_0131)
C0439231 (UMLS CUI 2011AA)
258706009 (SNOMED CT 2011_0131)
MO (HL7 V3 2006_05)
C0205360 (UMLS CUI 2011AA)
58158008 (SNOMED CT 2011_0131)
MTHU015276 (LOINC Version 232)
C0178602 (UMLS CUI 2011AA)
260911001 (SNOMED CT 2011_0131)
C0205448 (UMLS CUI 2011AA)
19338005 (SNOMED CT 2011_0131)
C0439231 (UMLS CUI 2011AA)
258706009 (SNOMED CT 2011_0131)
MO (HL7 V3 2006_05)
lower than recommended dose of EC-MPS (<1440g/day) due to gastrointestinal complaints.
Item
lower than recommended dose of EC-MPS (<1440g/day) due to gastrointestinal complaints.
boolean
C0547044 (UMLS CUI 2011AA)
263796003 (SNOMED CT 2011_0131)
C0034866 (UMLS CUI 2011AA)
MTHU036724 (LOINC Version 232)
RMD (HL7 V3 2006_05)
C0178602 (UMLS CUI 2011AA)
260911001 (SNOMED CT 2011_0131)
C0039226 (UMLS CUI 2011AA)
385059007 (SNOMED CT 2011_0131)
ECTAB (HL7 V3 2006_05)
C1337395 (UMLS CUI 2011AA)
426216009 (SNOMED CT 2011_0131)
CL420107 (UMLS CUI 2011AA)
C0521362 (UMLS CUI 2011AA)
MTHU031867 (LOINC Version 232)
C0277786 (UMLS CUI 2011AA)
33962009 (SNOMED CT 2011_0131)
MTHU001077 (LOINC Version 232)
Item Group
Ausschlusskriterien
CL425201 (UMLS CUI 2011AA)
patients who have participated in this study before
Item
patients who have participated in this study before
boolean
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
C0150312 (UMLS CUI 2011AA)
52101004 (SNOMED CT 2011_0131)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
patients currently participating in another clinical trial, or who participated in one during the last 30 days.
Item
patients currently participating in another clinical trial, or who participated in one during the last 30 days.
boolean
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)
C0521116 (UMLS CUI 2011AA)
15240007 (SNOMED CT 2011_0131)
CL414906 (UMLS CUI 2011AA)
C0347984 (UMLS CUI 2011AA)
371881003 (SNOMED CT 2011_0131)
C1517741 (UMLS CUI 2011AA)
C0439231 (UMLS CUI 2011AA)
258706009 (SNOMED CT 2011_0131)
MO (HL7 V3 2006_05)

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