ID

4476

Description

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

Lien

http://clinicaltrials.gov/show/NCT00420472

Mots-clés

Versions (1)
  1. 09/12/2013 09/12/2013 - Martin Dugas
Téléchargé le

9 décembre 2013

DOI

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Licence

Creative Commons BY 4.0
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Eligibility NCT00420472 Kidney Transplantation

Allemand Anglais

Eligibility

1 Formulaires  
  1. StudyEvent: Eligibility
    1. Eligibility
Einschlusskriterien
Description

Einschlusskriterien

Alias
UMLS CUI 2011AA
CL425202
Alter mindestens 18 Jahre
Description

age at least 18 Years

Type de données

boolean

Alias
UMLS CUI 2011AA
C0001779
SNOMED CT 2011_0131
397669002
Erwachsener, erwachsen
Description

adult patients, >=18 years of age

Type de données

boolean

Alias
UMLS CUI 2011AA
C0001675
SNOMED CT 2011_0131
133936004
first or second kidney transplant
Description

first or second kidney transplant

Type de données

boolean

Alias
UMLS CUI 2011AA
C0205435
SNOMED CT 2011_0131
255216001
UMLS CUI 2011AA
C0205436
SNOMED CT 2011_0131
81170007
UMLS CUI 2011AA
C0022671
SNOMED CT 2011_0131
70536003
MedDRA 14.1
10038533
ICD-9-CM Version 2011
55.6
UMLS CUI 2011AA
C0011900
SNOMED CT 2011_0131
439401001
LOINC Version 232
MTHU008876
EC-MPS therapy for >=6 months, with a stable dose for >=2 months
Description

EC-MPS therapy for >=6 months, with a stable dose for >=2 months

Type de données

boolean

Alias
UMLS CUI 2011AA
C0039226
SNOMED CT 2011_0131
385059007
HL7 V3 2006_05
ECTAB
UMLS CUI 2011AA
C1337395
SNOMED CT 2011_0131
426216009
UMLS CUI 2011AA
C0039798
UMLS CUI 2011AA
C0205452
SNOMED CT 2011_0131
68244004
UMLS CUI 2011AA
C0439231
SNOMED CT 2011_0131
258706009
HL7 V3 2006_05
MO
UMLS CUI 2011AA
C0205360
SNOMED CT 2011_0131
58158008
LOINC Version 232
MTHU015276
UMLS CUI 2011AA
C0178602
SNOMED CT 2011_0131
260911001
UMLS CUI 2011AA
C0205448
SNOMED CT 2011_0131
19338005
UMLS CUI 2011AA
C0439231
SNOMED CT 2011_0131
258706009
HL7 V3 2006_05
MO
lower than recommended dose of EC-MPS (<1440g/day) due to gastrointestinal complaints.
Description

lower than recommended dose of EC-MPS (<1440g/day) due to gastrointestinal complaints.

Type de données

boolean

Alias
UMLS CUI 2011AA
C0547044
SNOMED CT 2011_0131
263796003
UMLS CUI 2011AA
C0034866
LOINC Version 232
MTHU036724
HL7 V3 2006_05
RMD
UMLS CUI 2011AA
C0178602
SNOMED CT 2011_0131
260911001
UMLS CUI 2011AA
C0039226
SNOMED CT 2011_0131
385059007
HL7 V3 2006_05
ECTAB
UMLS CUI 2011AA
C1337395
SNOMED CT 2011_0131
426216009
UMLS CUI 2011AA
CL420107
UMLS CUI 2011AA
C0521362
LOINC Version 232
MTHU031867
UMLS CUI 2011AA
C0277786
SNOMED CT 2011_0131
33962009
LOINC Version 232
MTHU001077
Ausschlusskriterien
Description

Ausschlusskriterien

Alias
UMLS CUI 2011AA
CL425201
patients who have participated in this study before
Description

patients who have participated in this study before

Type de données

boolean

Alias
UMLS CUI 2011AA
C0332152
SNOMED CT 2011_0131
288556008
UMLS CUI 2011AA
C0679823
HL7 V3 2006_05
PART
UMLS CUI 2011AA
C0150312
SNOMED CT 2011_0131
52101004
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008
patients currently participating in another clinical trial, or who participated in one during the last 30 days.
Description

patients currently participating in another clinical trial, or who participated in one during the last 30 days.

Type de données

boolean

Alias
UMLS CUI 2011AA
C0679823
HL7 V3 2006_05
PART
UMLS CUI 2011AA
C0205394
SNOMED CT 2011_0131
74964007
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008
UMLS CUI 2011AA
C0521116
SNOMED CT 2011_0131
15240007
UMLS CUI 2011AA
CL414906
UMLS CUI 2011AA
C0347984
SNOMED CT 2011_0131
371881003
UMLS CUI 2011AA
C1517741
UMLS CUI 2011AA
C0439231
SNOMED CT 2011_0131
258706009
HL7 V3 2006_05
MO
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Similar models

Eligibility

1 Formulaires
  1. StudyEvent: Eligibility
    1. Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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