ID

3734

Beschreibung

ODM derived from http://clinicaltrials.gov/show/NCT01286779

Link

http://clinicaltrials.gov/show/NCT01286779

Stichworte

Versionen (2)
  1. 28.02.13 28.02.13 - Martin Dugas
  2. 20.09.21 20.09.21 -
Hochgeladen am

28. Februar 2013

DOI

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Eligibility NCT01286779 Hemophilia B

Deutsch Englisch

Eligibility

1 Formulare  
  1. StudyEvent: Eligibility
    1. Eligibility
Einschlusskriterien
Beschreibung

Einschlusskriterien

Alter 12 bis 65 Jahre
Beschreibung

age 12 Years to 65 Years

Datentyp

boolean

Alias
UMLS CUI 2011AA
C0001779
SNOMED CT 2011_0131
397669002
Subject and/or legal representative has/have voluntarily provided signed informed consent
Beschreibung

Subject and/or legal representative has/have voluntarily provided signed informed consent

Datentyp

boolean

Alias
UMLS CUI 2011AA
C0681850
UMLS CUI 2011AA
C1301860
SNOMED CT 2011_0131
398165009
UMLS CUI 2011AA
C0030701
UMLS CUI 2011AA
C1709695
UMLS CUI 2011AA
C1519316
UMLS CUI 2011AA
C0021430
Subject has completed Baxter clinical study 250901
Beschreibung

Subject has completed Baxter clinical study 250901

Datentyp

boolean

Alias
UMLS CUI 2011AA
C0681850
UMLS CUI 2011AA
C1556116
HL7 V3 2006_05
completed
UMLS CUI 2011AA
C0332152
SNOMED CT 2011_0131
288556008
UMLS CUI 2011AA
C1552884
HL7 V3 2006_05
BA
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008
Subject has severe (FIX level < 1%) or moderately severe (FIX level <= 2%) hemophilia B (based on the one stage activated partial thromboplastin time (aPTT) assay), as tested at screening at the central laboratory
Beschreibung

Subject has severe (FIX level < 1%) or moderately severe (FIX level <= 2%) hemophilia B (based on the one stage activated partial thromboplastin time (aPTT) assay), as tested at screening at the central laboratory

Datentyp

boolean

Alias
UMLS CUI 2011AA
C0200408
SNOMED CT 2011_0131
78882004
MedDRA 14.1
10009744
UMLS CUI 2011AA
C0205082
SNOMED CT 2011_0131
24484000
UMLS CUI 2011AA
C1299393
SNOMED CT 2011_0131
371924009
UMLS CUI 2011AA
C0008533
SNOMED CT 2011_0131
41788008
MedDRA 14.1
10016077
ICD-10-CM Version 2010
D67
ICD-9-CM Version 2011
286.1
UMLS CUI 2011AA
C0011900
SNOMED CT 2011_0131
439401001
LOINC Version 232
MTHU008876
UMLS CUI 2011AA
C0030605
SNOMED CT 2011_0131
42525009
MedDRA 14.1
10000630
Subject has not developed an inhibitory FIX antibody during Baxter clinical study 250901
Beschreibung

Subject has not developed an inhibitory FIX antibody during Baxter clinical study 250901

Datentyp

boolean

Alias
UMLS CUI 2011AA
C1518422
UMLS CUI 2011AA
C1511795
UMLS CUI 2011AA
C0302077
SNOMED CT 2011_0131
36020009
UMLS CUI 2011AA
C0347984
SNOMED CT 2011_0131
371881003
UMLS CUI 2011AA
C0332152
SNOMED CT 2011_0131
288556008
UMLS CUI 2011AA
C1552884
HL7 V3 2006_05
BA
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008
Ausschlusskriterien
Beschreibung

Ausschlusskriterien

Subject received factor IX product(s) other than BAX 326 upon completion of Baxter protocol 250901
Beschreibung

Subject received factor IX product(s) other than BAX 326 upon completion of Baxter protocol 250901

Datentyp

boolean

Alias
UMLS CUI 2011AA
C1514756
UMLS CUI 2011AA
C1827657
SNOMED CT 2011_0131
424562004
UMLS CUI 2011AA
CL411789
UMLS CUI 2011AA
C0332152
SNOMED CT 2011_0131
288556008
UMLS CUI 2011AA
C1552884
HL7 V3 2006_05
BA
UMLS CUI 2011AA
C1514468
Subject has been diagnosed with an acquired hemostatic defect other than hemophilia B
Beschreibung

Subject has been diagnosed with an acquired hemostatic defect other than hemophilia B

Datentyp

boolean

Alias
UMLS CUI 2011AA
C0011900
SNOMED CT 2011_0131
439401001
LOINC Version 232
MTHU008876
UMLS CUI 2011AA
C0439661
SNOMED CT 2011_0131
255396000
UMLS CUI 2011AA
C0019116
SNOMED CT 2011_0131
74848003
UMLS CUI 2011AA
C1457869
SNOMED CT 2011_0131
6920004
UMLS CUI 2011AA
CL411789
UMLS CUI 2011AA
C0008533
SNOMED CT 2011_0131
41788008
MedDRA 14.1
10016077
ICD-10-CM Version 2010
D67
ICD-9-CM Version 2011
286.1
Körpergewicht
Beschreibung

Subject's weight is < 35 kg or > 120 kg

Datentyp

boolean

Alias
UMLS CUI 2011AA
C0005910
SNOMED CT 2011_0131
27113001
LOINC Version 232
MTHU001885
Subject is planned to take part in any other clinical study, with the exception of BAX 326 Surgery study as described in this protocol, during the course of the continuation study
Beschreibung

Subject is planned to take part in any other clinical study, with the exception of BAX 326 Surgery study as described in this protocol, during the course of the continuation study

Datentyp

boolean

Alias
UMLS CUI 2011AA
C1301732
SNOMED CT 2011_0131
397943006
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
C1554961
HL7 V3 2006_05
E
UMLS CUI 2011AA
C0332152
SNOMED CT 2011_0131
288556008
UMLS CUI 2011AA
C1552884
HL7 V3 2006_05
BA
UMLS CUI 2011AA
C0038895
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility

1 Formulare
  1. StudyEvent: Eligibility
    1. Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Einschlusskriterien
age 12 Years to 65 Years
Item
Alter 12 bis 65 Jahre
boolean
C0001779 (UMLS CUI 2011AA)
397669002 (SNOMED CT 2011_0131)
Subject and/or legal representative has/have voluntarily provided signed informed consent
Item
Subject and/or legal representative has/have voluntarily provided signed informed consent
boolean
C0681850 (UMLS CUI 2011AA)
C1301860 (UMLS CUI 2011AA)
398165009 (SNOMED CT 2011_0131)
C0030701 (UMLS CUI 2011AA)
C1709695 (UMLS CUI 2011AA)
C1519316 (UMLS CUI 2011AA)
C0021430 (UMLS CUI 2011AA)
Subject has completed Baxter clinical study 250901
Item
Subject has completed Baxter clinical study 250901
boolean
C0681850 (UMLS CUI 2011AA)
C1556116 (UMLS CUI 2011AA)
completed (HL7 V3 2006_05)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C1552884 (UMLS CUI 2011AA)
BA (HL7 V3 2006_05)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
Subject has severe (FIX level < 1%) or moderately severe (FIX level <= 2%) hemophilia B (based on the one stage activated partial thromboplastin time (aPTT) assay), as tested at screening at the central laboratory
Item
Subject has severe (FIX level < 1%) or moderately severe (FIX level <= 2%) hemophilia B (based on the one stage activated partial thromboplastin time (aPTT) assay), as tested at screening at the central laboratory
boolean
C0200408 (UMLS CUI 2011AA)
78882004 (SNOMED CT 2011_0131)
10009744 (MedDRA 14.1)
C0205082 (UMLS CUI 2011AA)
24484000 (SNOMED CT 2011_0131)
C1299393 (UMLS CUI 2011AA)
371924009 (SNOMED CT 2011_0131)
C0008533 (UMLS CUI 2011AA)
41788008 (SNOMED CT 2011_0131)
10016077 (MedDRA 14.1)
D67 (ICD-10-CM Version 2010)
286.1 (ICD-9-CM Version 2011)
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
C0030605 (UMLS CUI 2011AA)
42525009 (SNOMED CT 2011_0131)
10000630 (MedDRA 14.1)
Subject has not developed an inhibitory FIX antibody during Baxter clinical study 250901
Item
Subject has not developed an inhibitory FIX antibody during Baxter clinical study 250901
boolean
C1518422 (UMLS CUI 2011AA)
C1511795 (UMLS CUI 2011AA)
C0302077 (UMLS CUI 2011AA)
36020009 (SNOMED CT 2011_0131)
C0347984 (UMLS CUI 2011AA)
371881003 (SNOMED CT 2011_0131)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C1552884 (UMLS CUI 2011AA)
BA (HL7 V3 2006_05)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
Item Group
Ausschlusskriterien
Subject received factor IX product(s) other than BAX 326 upon completion of Baxter protocol 250901
Item
Subject received factor IX product(s) other than BAX 326 upon completion of Baxter protocol 250901
boolean
C1514756 (UMLS CUI 2011AA)
C1827657 (UMLS CUI 2011AA)
424562004 (SNOMED CT 2011_0131)
CL411789 (UMLS CUI 2011AA)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C1552884 (UMLS CUI 2011AA)
BA (HL7 V3 2006_05)
C1514468 (UMLS CUI 2011AA)
Subject has been diagnosed with an acquired hemostatic defect other than hemophilia B
Item
Subject has been diagnosed with an acquired hemostatic defect other than hemophilia B
boolean
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
C0439661 (UMLS CUI 2011AA)
255396000 (SNOMED CT 2011_0131)
C0019116 (UMLS CUI 2011AA)
74848003 (SNOMED CT 2011_0131)
C1457869 (UMLS CUI 2011AA)
6920004 (SNOMED CT 2011_0131)
CL411789 (UMLS CUI 2011AA)
C0008533 (UMLS CUI 2011AA)
41788008 (SNOMED CT 2011_0131)
10016077 (MedDRA 14.1)
D67 (ICD-10-CM Version 2010)
286.1 (ICD-9-CM Version 2011)
Subject's weight is < 35 kg or > 120 kg
Item
Körpergewicht
boolean
C0005910 (UMLS CUI 2011AA)
27113001 (SNOMED CT 2011_0131)
MTHU001885 (LOINC Version 232)
Subject is planned to take part in any other clinical study, with the exception of BAX 326 Surgery study as described in this protocol, during the course of the continuation study
Item
Subject is planned to take part in any other clinical study, with the exception of BAX 326 Surgery study as described in this protocol, during the course of the continuation study
boolean
C1301732 (UMLS CUI 2011AA)
397943006 (SNOMED CT 2011_0131)
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)
C1554961 (UMLS CUI 2011AA)
E (HL7 V3 2006_05)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C1552884 (UMLS CUI 2011AA)
BA (HL7 V3 2006_05)
C0038895 (UMLS CUI 2011AA)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
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