ID
42782
Description
ODM derived from http://clinicaltrials.gov/show/NCT00409175
Link
http://clinicaltrials.gov/show/NCT00409175
Keywords
Versions (2)
- 12/9/13 12/9/13 - Martin Dugas
- 9/17/21 9/17/21 -
Uploaded on
September 17, 2021
DOI
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License
Creative Commons BY 4.0
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Eligibility NCT00409175 Familial Amyloid Polyneuropathy
Eligibility
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI 2011AA
- CL425201
Description
Chronic use of non-steroidal anti-inflammatory drugs (NSAIDs).
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0205191
- SNOMED CT 2011_0131
- 90734009
- UMLS CUI 2011AA
- C1524063
- SNOMED CT 2011_0131
- 260676000
- UMLS CUI 2011AA
- C0003211
- SNOMED CT 2011_0131
- 16403005
Description
Primary amyloidosis.
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0268381
- SNOMED CT 2011_0131
- 23132008
- MedDRA 14.1
- 10036673
Description
If female, patient is pregnant or breast feeding.
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0086287
- SNOMED CT 2011_0131
- 248152002
- HL7 V3 2006_05
- F
- UMLS CUI 2011AA
- C0549206
- MedDRA 14.1
- 10036586
- UMLS CUI 2011AA
- C0006147
- MedDRA 14.1
- 10006247
Description
Prior liver transplantation.
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C0023911
- SNOMED CT 2011_0131
- 18027006
- MedDRA 14.1
- 10024714
- ICD-9-CM Version 2011
- 50.5
Description
No recordable sensory threshold for vibration perception in both feet, as measured by CASE IV.
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0443341
- SNOMED CT 2011_0131
- 263920009
- UMLS CUI 2011AA
- C0036677
- SNOMED CT 2011_0131
- 246511009
- UMLS CUI 2011AA
- C0597644
- UMLS CUI 2011AA
- C0230473
- SNOMED CT 2011_0131
- 8580001
- LOINC Version 232
- MTHU012589
- UMLS CUI 2011AA
- C0444706
- SNOMED CT 2011_0131
- 258104002
- UMLS CUI 2011AA
- C0009622
- UMLS CUI 2011AA
- CL420230
- UMLS CUI 2011AA
- C0445254
- SNOMED CT 2011_0131
- 262139008
- UMLS CUI 2011AA
- C0220825
- UMLS CUI 2011AA
- C0677510
- SNOMED CT 2011_0131
- 260317009
Description
Positive results for hepatitis B surface antigen (HBsAg), anti-hepatitis C virus (HCV), and/or human immunodeficiency virus (HIV).
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0149709
- SNOMED CT 2011_0131
- 165806002
- MedDRA 14.1
- 10019742
- UMLS CUI 2011AA
- C0281863
- MedDRA 14.1
- 10019747
- UMLS CUI 2011AA
- C0019699
- SNOMED CT 2011_0131
- 165816005
- MedDRA 14.1
- 10020188
- ICD-10-CM Version 2010
- Z21
Description
Renal insufficiency or liver function test abnormalities.
Data type
boolean
Alias
- UMLS CUI 2011AA
- C1565489
- MedDRA 14.1
- 10038474
- UMLS CUI 2011AA
- C0151766
- SNOMED CT 2011_0131
- 166603001
- MedDRA 14.1
- 10024690
- ICD-10-CM Version 2010
- R94.5
- ICD-9-CM Version 2011
- 794.8
Description
New York Heart Association (NYHA) Functional Classification ≥III.
Data type
boolean
Alias
- UMLS CUI 2011AA
- C1319795
- SNOMED CT 2011_0131
- 420913000
- MedDRA 14.1
- 10064081
- UMLS CUI 2011AA
- C1319796
- SNOMED CT 2011_0131
- 422293003
- MedDRA 14.1
- 10064082
Description
Other causes of sensorimotor neuropathy (B12 deficiency, Diabetes Mellitus, HIV treated with retroviral medications, thyroid disorders, alcohol abuse, and chronic inflammatory diseases).
Data type
boolean
Alias
- UMLS CUI 2011AA
- C1112256
- MedDRA 14.1
- 10056673
- UMLS CUI 2011AA
- C0205394
- SNOMED CT 2011_0131
- 74964007
- UMLS CUI 2011AA
- C1314792
- SNOMED CT 2011_0131
- 134198009
- UMLS CUI 2011AA
- C0042847
- SNOMED CT 2011_0131
- 190634004
- MedDRA 14.1
- 10047609
- ICD-10-CM Version 2010
- E53.8
- UMLS CUI 2011AA
- C0011849
- SNOMED CT 2011_0131
- 191044006
- UMLS CUI 2011AA
- C0019682
- SNOMED CT 2011_0131
- 19030005
- UMLS CUI 2011AA
- CL415147
- UMLS CUI 2011AA
- CL106887
- UMLS CUI 2011AA
- C0013227
- UMLS CUI 2011AA
- C0040128
- SNOMED CT 2011_0131
- 14304000
- MedDRA 14.1
- 10043709
- ICD-10-CM Version 2010
- E00-E07
- ICD-9-CM Version 2011
- 240-246.99
- UMLS CUI 2011AA
- C0085762
- SNOMED CT 2011_0131
- 15167005
- MedDRA 14.1
- 10001584
- LOINC Version 232
- LP36309-0
- ICD-10-CM Version 2010
- F10.1
- ICD-9-CM Version 2011
- 305.0
- UMLS CUI 2011AA
- C1290886
- SNOMED CT 2011_0131
- 128294001
Description
Co-morbidity anticipated to limit survival to < 18 months.
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0009488
- UMLS CUI 2011AA
- C0679106
- UMLS CUI 2011AA
- C2349209
- UMLS CUI 2011AA
- C0220921
- UMLS CUI 2011AA
- C0439231
- SNOMED CT 2011_0131
- 258706009
- HL7 V3 2006_05
- MO
Description
Patient received an investigational drug/device and/or participated in another clinical investigational study within 60 days before Baseline.
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0030705
- SNOMED CT 2011_0131
- 116154003
- UMLS CUI 2011AA
- C1514756
- UMLS CUI 2011AA
- C0013230
- UMLS CUI 2011AA
- C2346570
- UMLS CUI 2011AA
- C0679823
- HL7 V3 2006_05
- PART
- UMLS CUI 2011AA
- C0205394
- SNOMED CT 2011_0131
- 74964007
- UMLS CUI 2011AA
- C1517586
- UMLS CUI 2011AA
- C0008976
- SNOMED CT 2011_0131
- 110465008
- UMLS CUI 2011AA
- C0205448
- SNOMED CT 2011_0131
- 19338005
- UMLS CUI 2011AA
- C0439231
- SNOMED CT 2011_0131
- 258706009
- HL7 V3 2006_05
- MO
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C1442488
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