ID

42845

Descripción

ODM derived from http://clinicaltrials.gov/show/NCT00241514

Link

http://clinicaltrials.gov/show/NCT00241514

Palabras clave

  1. 11/12/13 11/12/13 - Martin Dugas
  2. 17/9/21 17/9/21 -
Subido en

17 de septiembre de 2021

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0

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Eligibility NCT00241514 GERD

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Einschlusskriterien
Descripción

Einschlusskriterien

Alias
UMLS CUI 2011AA
CL425202
Alter 18 Jahre und älter
Descripción

age >=18 Years

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0001779
SNOMED CT 2011_0131
397669002
Signed informed consent.
Descripción

Signed informed consent.

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C1561610
HL7 V3 2006_05
S
UMLS CUI 2011AA
C0021430
Completed the SH-NEN-0001 study with relief of upper GI symptom. Relief is defined as "last 7 days with a diary assessment of None or Minimal, but allowing up to 2 days to be rated as Mild during the 7-day period".
Descripción

Completed the SH-NEN-0001 study with relief of upper GI symptom. Relief is defined as "last 7 days with a diary assessment of None or Minimal, but allowing up to 2 days to be rated as Mild during the 7-day period".

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0205197
SNOMED CT 2011_0131
255594003
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008
UMLS CUI 2011AA
C0564405
SNOMED CT 2011_0131
224978009
UMLS CUI 2011AA
C0203057
SNOMED CT 2011_0131
241157000
MedDRA 14.1
10046285
ICD-9-CM Version 2011
87.62
UMLS CUI 2011AA
C1457887
LOINC Version 232
MTHU021540
ICD-9-CM Version 2011
780-789.99
UMLS CUI 2011AA
C0376660
UMLS CUI 2011AA
C1516048
UMLS CUI 2011AA
C0549184
SNOMED CT 2011_0131
260413007
UMLS CUI 2011AA
C0547040
SNOMED CT 2011_0131
255605001
UMLS CUI 2011AA
C0871208
UMLS CUI 2011AA
C2945599
SNOMED CT 2011_0131
255604002
UMLS CUI 2011AA
C0347984
SNOMED CT 2011_0131
371881003
UMLS CUI 2011AA
C0439230
SNOMED CT 2011_0131
258705008
HL7 V3 2006_05
WK
UMLS CUI 2011AA
C1948053
A clinical diagnosis of a chronic condition (e.g., osteoarthritis or rheumatoid arthritis) that requires continuous daily NSAID treatment for at least 6 months. Daily NSAID treatment is defined as taking the prescribed dose for at least 5 of 7 days in any given week and can include COX-2 selective NSAIDs, multiple NSAIDs, and high-dose NSAIDs.
Descripción

A clinical diagnosis of a chronic condition (e.g., osteoarthritis or rheumatoid arthritis) that requires continuous daily NSAID treatment for at least 6 months. Daily NSAID treatment is defined as taking the prescribed dose for at least 5 of 7 days in any given week and can include COX-2 selective NSAIDs, multiple NSAIDs, and high-dose NSAIDs.

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0011900
SNOMED CT 2011_0131
439401001
LOINC Version 232
MTHU008876
UMLS CUI 2011AA
C0332140
SNOMED CT 2011_0131
39154008
UMLS CUI 2011AA
C0205191
SNOMED CT 2011_0131
90734009
UMLS CUI 2011AA
C0348080
SNOMED CT 2011_0131
260905004
HL7 V3 2006_05
COND
UMLS CUI 2011AA
C0029408
SNOMED CT 2011_0131
396275006, 225655006
MedDRA 14.1
10031161
ICD-10-CM Version 2010
M19.9
ICD-9-CM Version 2011
715.9
UMLS CUI 2011AA
C0003873
SNOMED CT 2011_0131
69896004
MedDRA 14.1
10039073
ICD-10-CM Version 2010
M06.9
ICD-9-CM Version 2011
714.0
UMLS CUI 2011AA
C1514873
UMLS CUI 2011AA
C0549178
UMLS CUI 2011AA
C0332173
SNOMED CT 2011_0131
69620002
UMLS CUI 2011AA
C0003211
SNOMED CT 2011_0131
16403005
UMLS CUI 2011AA
C0039798
UMLS CUI 2011AA
C1704788
UMLS CUI 2011AA
C0033080
SNOMED CT 2011_0131
16076005
UMLS CUI 2011AA
C0178602
SNOMED CT 2011_0131
260911001
UMLS CUI 2011AA
C1257954
SNOMED CT 2011_0131
387050005
UMLS CUI 2011AA
C0439064
SNOMED CT 2011_0131
255204007
UMLS CUI 2011AA
C0205250
SNOMED CT 2011_0131
75540009
UMLS CUI 2011AA
C0178602
SNOMED CT 2011_0131
260911001
Daily NSAID treatment dose and type: (Must have been stable for at least 9 weeks prior to inclusion and. Are expected to remain stable for the duration of the study. and. Must be administered orally. If more than one type of NSAID treatment is used, at least one type must be administered orally).
Descripción

Daily NSAID treatment dose and type: (Must have been stable for at least 9 weeks prior to inclusion and. Are expected to remain stable for the duration of the study. and. Must be administered orally. If more than one type of NSAID treatment is used, at least one type must be administered orally).

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0332173
SNOMED CT 2011_0131
69620002
UMLS CUI 2011AA
C0003211
SNOMED CT 2011_0131
16403005
UMLS CUI 2011AA
C0039798
UMLS CUI 2011AA
C0178602
SNOMED CT 2011_0131
260911001
UMLS CUI 2011AA
C0814259
UMLS CUI 2011AA
C0205360
SNOMED CT 2011_0131
58158008
LOINC Version 232
MTHU015276
UMLS CUI 2011AA
C0439230
SNOMED CT 2011_0131
258705008
HL7 V3 2006_05
WK
UMLS CUI 2011AA
C0332152
SNOMED CT 2011_0131
288556008
UMLS CUI 2011AA
CL425202
UMLS CUI 2011AA
C1517001
UMLS CUI 2011AA
C0449238
SNOMED CT 2011_0131
103335007
LOINC Version 232
MTHU001938
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008
UMLS CUI 2011AA
C1273553
SNOMED CT 2011_0131
394899003
Hp negative on Histology performed at baseline endoscopy in the study SHNEN- 0001.
Descripción

Hp negative on Histology performed at baseline endoscopy in the study SHNEN- 0001.

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0079488
SNOMED CT 2011_0131
80774000
LOINC Version 232
MTHU019876
UMLS CUI 2011AA
CL415098
UMLS CUI 2011AA
C0344441
MedDRA 14.1
10062005
LOINC Version 232
MTHU010496
UMLS CUI 2011AA
C1882330
UMLS CUI 2011AA
C1442488
UMLS CUI 2011AA
C0014245
SNOMED CT 2011_0131
423827005
MedDRA 14.1
10014805
LOINC Version 232
MTHU008659
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008
Ausschlusskriterien
Descripción

Ausschlusskriterien

Alias
UMLS CUI 2011AA
CL425201
Discontinuation from study SH-NEN-0001
Descripción

Discontinuation from study SH-NEN-0001

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0457454
SNOMED CT 2011_0131
278308006
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008
Pain, discomfort or burning in the upper abdomen precipitated by exercise or relieved by defecation.
Descripción

Pain, discomfort or burning in the upper abdomen precipitated by exercise or relieved by defecation.

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0030193
SNOMED CT 2011_0131
22253000
MedDRA 14.1
10033371
LOINC Version 232
MTHU029813
ICD-10-CM Version 2010
R52
ICD-9-CM Version 2011
338-338.9
CTCAE 1105E
E11167
UMLS CUI 2011AA
CL355048
SNOMED CT 2011_0131
247347003
UMLS CUI 2011AA
C0085624
SNOMED CT 2011_0131
90673000
MedDRA 14.1
10006784
UMLS CUI 2011AA
C2937240
SNOMED CT 2011_0131
80581009
UMLS CUI 2011AA
C1444748
SNOMED CT 2011_0131
410658008
UMLS CUI 2011AA
C0015259
SNOMED CT 2011_0131
256235009
MedDRA 14.1
10015634
UMLS CUI 2011AA
C0332303
SNOMED CT 2011_0131
1241001
UMLS CUI 2011AA
C0011135
SNOMED CT 2011_0131
39211005
Pain, discomfort or burning in the upper abdomen not associated with the use of NSAIDs, including COX-2 selective NSAIDs.
Descripción

Pain, discomfort or burning in the upper abdomen not associated with the use of NSAIDs, including COX-2 selective NSAIDs.

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0030193
SNOMED CT 2011_0131
22253000
MedDRA 14.1
10033371
LOINC Version 232
MTHU029813
ICD-10-CM Version 2010
R52
ICD-9-CM Version 2011
338-338.9
CTCAE 1105E
E11167
UMLS CUI 2011AA
CL355048
SNOMED CT 2011_0131
247347003
UMLS CUI 2011AA
C0085624
SNOMED CT 2011_0131
90673000
MedDRA 14.1
10006784
UMLS CUI 2011AA
C2937240
SNOMED CT 2011_0131
80581009
UMLS CUI 2011AA
C1518422
UMLS CUI 2011AA
C0332281
SNOMED CT 2011_0131
47429007
UMLS CUI 2011AA
C1524063
SNOMED CT 2011_0131
260676000
UMLS CUI 2011AA
C0003211
SNOMED CT 2011_0131
16403005
UMLS CUI 2011AA
C0332257
SNOMED CT 2011_0131
55919000
UMLS CUI 2011AA
C1257954
SNOMED CT 2011_0131
387050005
Pregnancy or lactation. Women of childbearing potential must maintain effective contraception during the study period as judged by the investigator.
Descripción

Pregnancy or lactation. Women of childbearing potential must maintain effective contraception during the study period as judged by the investigator.

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0032961
SNOMED CT 2011_0131
289908002
MedDRA 14.1
10036556
LOINC Version 232
MTHU035048
UMLS CUI 2011AA
C0006147
MedDRA 14.1
10006247
UMLS CUI 2011AA
C0043210
SNOMED CT 2011_0131
224526002
UMLS CUI 2011AA
C1148523
UMLS CUI 2011AA
C0237399
UMLS CUI 2011AA
C0024501
UMLS CUI 2011AA
C1704419
SNOMED CT 2011_0131
254648000
UMLS CUI 2011AA
C0700589
SNOMED CT 2011_0131
146680009
MedDRA 14.1
10010808
UMLS CUI 2011AA
C0347984
SNOMED CT 2011_0131
371881003
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008
UMLS CUI 2011AA
C1948053
UMLS CUI 2011AA
C0022423
SNOMED CT 2011_0131
61254005
UMLS CUI 2011AA
CL102947
Need for continuous concomitant therapy with: (Anticoagulants, Corticosteroids at doses higher than explained under inclusion criterion)
Descripción

Need for continuous concomitant therapy with: (Anticoagulants, Corticosteroids at doses higher than explained under inclusion criterion)

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0686904
SNOMED CT 2011_0131
103325001
UMLS CUI 2011AA
C0549178
UMLS CUI 2011AA
C1707479
UMLS CUI 2011AA
C0003280
SNOMED CT 2011_0131
372862008
UMLS CUI 2011AA
C0001617
SNOMED CT 2011_0131
79440004
UMLS CUI 2011AA
C0178602
SNOMED CT 2011_0131
260911001
UMLS CUI 2011AA
C0444956
SNOMED CT 2011_0131
261829003
UMLS CUI 2011AA
C0681841
LOINC Version 232
MTHU013812
UMLS CUI 2011AA
CL425202

Similar models

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Einschlusskriterien
CL425202 (UMLS CUI 2011AA)
age >=18 Years
Item
Alter 18 Jahre und älter
boolean
C0001779 (UMLS CUI 2011AA)
397669002 (SNOMED CT 2011_0131)
Signed informed consent.
Item
Signed informed consent.
boolean
C1561610 (UMLS CUI 2011AA)
S (HL7 V3 2006_05)
C0021430 (UMLS CUI 2011AA)
Completed the SH-NEN-0001 study with relief of upper GI symptom. Relief is defined as "last 7 days with a diary assessment of None or Minimal, but allowing up to 2 days to be rated as Mild during the 7-day period".
Item
Completed the SH-NEN-0001 study with relief of upper GI symptom. Relief is defined as "last 7 days with a diary assessment of None or Minimal, but allowing up to 2 days to be rated as Mild during the 7-day period".
boolean
C0205197 (UMLS CUI 2011AA)
255594003 (SNOMED CT 2011_0131)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
C0564405 (UMLS CUI 2011AA)
224978009 (SNOMED CT 2011_0131)
C0203057 (UMLS CUI 2011AA)
241157000 (SNOMED CT 2011_0131)
10046285 (MedDRA 14.1)
87.62 (ICD-9-CM Version 2011)
C1457887 (UMLS CUI 2011AA)
MTHU021540 (LOINC Version 232)
780-789.99 (ICD-9-CM Version 2011)
C0376660 (UMLS CUI 2011AA)
C1516048 (UMLS CUI 2011AA)
C0549184 (UMLS CUI 2011AA)
260413007 (SNOMED CT 2011_0131)
C0547040 (UMLS CUI 2011AA)
255605001 (SNOMED CT 2011_0131)
C0871208 (UMLS CUI 2011AA)
C2945599 (UMLS CUI 2011AA)
255604002 (SNOMED CT 2011_0131)
C0347984 (UMLS CUI 2011AA)
371881003 (SNOMED CT 2011_0131)
C0439230 (UMLS CUI 2011AA)
258705008 (SNOMED CT 2011_0131)
WK (HL7 V3 2006_05)
C1948053 (UMLS CUI 2011AA)
A clinical diagnosis of a chronic condition (e.g., osteoarthritis or rheumatoid arthritis) that requires continuous daily NSAID treatment for at least 6 months. Daily NSAID treatment is defined as taking the prescribed dose for at least 5 of 7 days in any given week and can include COX-2 selective NSAIDs, multiple NSAIDs, and high-dose NSAIDs.
Item
A clinical diagnosis of a chronic condition (e.g., osteoarthritis or rheumatoid arthritis) that requires continuous daily NSAID treatment for at least 6 months. Daily NSAID treatment is defined as taking the prescribed dose for at least 5 of 7 days in any given week and can include COX-2 selective NSAIDs, multiple NSAIDs, and high-dose NSAIDs.
boolean
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
C0332140 (UMLS CUI 2011AA)
39154008 (SNOMED CT 2011_0131)
C0205191 (UMLS CUI 2011AA)
90734009 (SNOMED CT 2011_0131)
C0348080 (UMLS CUI 2011AA)
260905004 (SNOMED CT 2011_0131)
COND (HL7 V3 2006_05)
C0029408 (UMLS CUI 2011AA)
396275006, 225655006 (SNOMED CT 2011_0131)
10031161 (MedDRA 14.1)
M19.9 (ICD-10-CM Version 2010)
715.9 (ICD-9-CM Version 2011)
C0003873 (UMLS CUI 2011AA)
69896004 (SNOMED CT 2011_0131)
10039073 (MedDRA 14.1)
M06.9 (ICD-10-CM Version 2010)
714.0 (ICD-9-CM Version 2011)
C1514873 (UMLS CUI 2011AA)
C0549178 (UMLS CUI 2011AA)
C0332173 (UMLS CUI 2011AA)
69620002 (SNOMED CT 2011_0131)
C0003211 (UMLS CUI 2011AA)
16403005 (SNOMED CT 2011_0131)
C0039798 (UMLS CUI 2011AA)
C1704788 (UMLS CUI 2011AA)
C0033080 (UMLS CUI 2011AA)
16076005 (SNOMED CT 2011_0131)
C0178602 (UMLS CUI 2011AA)
260911001 (SNOMED CT 2011_0131)
C1257954 (UMLS CUI 2011AA)
387050005 (SNOMED CT 2011_0131)
C0439064 (UMLS CUI 2011AA)
255204007 (SNOMED CT 2011_0131)
C0205250 (UMLS CUI 2011AA)
75540009 (SNOMED CT 2011_0131)
C0178602 (UMLS CUI 2011AA)
260911001 (SNOMED CT 2011_0131)
Daily NSAID treatment dose and type: (Must have been stable for at least 9 weeks prior to inclusion and. Are expected to remain stable for the duration of the study. and. Must be administered orally. If more than one type of NSAID treatment is used, at least one type must be administered orally).
Item
Daily NSAID treatment dose and type: (Must have been stable for at least 9 weeks prior to inclusion and. Are expected to remain stable for the duration of the study. and. Must be administered orally. If more than one type of NSAID treatment is used, at least one type must be administered orally).
boolean
C0332173 (UMLS CUI 2011AA)
69620002 (SNOMED CT 2011_0131)
C0003211 (UMLS CUI 2011AA)
16403005 (SNOMED CT 2011_0131)
C0039798 (UMLS CUI 2011AA)
C0178602 (UMLS CUI 2011AA)
260911001 (SNOMED CT 2011_0131)
C0814259 (UMLS CUI 2011AA)
C0205360 (UMLS CUI 2011AA)
58158008 (SNOMED CT 2011_0131)
MTHU015276 (LOINC Version 232)
C0439230 (UMLS CUI 2011AA)
258705008 (SNOMED CT 2011_0131)
WK (HL7 V3 2006_05)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
CL425202 (UMLS CUI 2011AA)
C1517001 (UMLS CUI 2011AA)
C0449238 (UMLS CUI 2011AA)
103335007 (SNOMED CT 2011_0131)
MTHU001938 (LOINC Version 232)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
C1273553 (UMLS CUI 2011AA)
394899003 (SNOMED CT 2011_0131)
Hp negative on Histology performed at baseline endoscopy in the study SHNEN- 0001.
Item
Hp negative on Histology performed at baseline endoscopy in the study SHNEN- 0001.
boolean
C0079488 (UMLS CUI 2011AA)
80774000 (SNOMED CT 2011_0131)
MTHU019876 (LOINC Version 232)
CL415098 (UMLS CUI 2011AA)
C0344441 (UMLS CUI 2011AA)
10062005 (MedDRA 14.1)
MTHU010496 (LOINC Version 232)
C1882330 (UMLS CUI 2011AA)
C1442488 (UMLS CUI 2011AA)
C0014245 (UMLS CUI 2011AA)
423827005 (SNOMED CT 2011_0131)
10014805 (MedDRA 14.1)
MTHU008659 (LOINC Version 232)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
Item Group
Ausschlusskriterien
CL425201 (UMLS CUI 2011AA)
Discontinuation from study SH-NEN-0001
Item
Discontinuation from study SH-NEN-0001
boolean
C0457454 (UMLS CUI 2011AA)
278308006 (SNOMED CT 2011_0131)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
Pain, discomfort or burning in the upper abdomen precipitated by exercise or relieved by defecation.
Item
Pain, discomfort or burning in the upper abdomen precipitated by exercise or relieved by defecation.
boolean
C0030193 (UMLS CUI 2011AA)
22253000 (SNOMED CT 2011_0131)
10033371 (MedDRA 14.1)
MTHU029813 (LOINC Version 232)
R52 (ICD-10-CM Version 2010)
338-338.9 (ICD-9-CM Version 2011)
E11167 (CTCAE 1105E)
CL355048 (UMLS CUI 2011AA)
247347003 (SNOMED CT 2011_0131)
C0085624 (UMLS CUI 2011AA)
90673000 (SNOMED CT 2011_0131)
10006784 (MedDRA 14.1)
C2937240 (UMLS CUI 2011AA)
80581009 (SNOMED CT 2011_0131)
C1444748 (UMLS CUI 2011AA)
410658008 (SNOMED CT 2011_0131)
C0015259 (UMLS CUI 2011AA)
256235009 (SNOMED CT 2011_0131)
10015634 (MedDRA 14.1)
C0332303 (UMLS CUI 2011AA)
1241001 (SNOMED CT 2011_0131)
C0011135 (UMLS CUI 2011AA)
39211005 (SNOMED CT 2011_0131)
Pain, discomfort or burning in the upper abdomen not associated with the use of NSAIDs, including COX-2 selective NSAIDs.
Item
Pain, discomfort or burning in the upper abdomen not associated with the use of NSAIDs, including COX-2 selective NSAIDs.
boolean
C0030193 (UMLS CUI 2011AA)
22253000 (SNOMED CT 2011_0131)
10033371 (MedDRA 14.1)
MTHU029813 (LOINC Version 232)
R52 (ICD-10-CM Version 2010)
338-338.9 (ICD-9-CM Version 2011)
E11167 (CTCAE 1105E)
CL355048 (UMLS CUI 2011AA)
247347003 (SNOMED CT 2011_0131)
C0085624 (UMLS CUI 2011AA)
90673000 (SNOMED CT 2011_0131)
10006784 (MedDRA 14.1)
C2937240 (UMLS CUI 2011AA)
80581009 (SNOMED CT 2011_0131)
C1518422 (UMLS CUI 2011AA)
C0332281 (UMLS CUI 2011AA)
47429007 (SNOMED CT 2011_0131)
C1524063 (UMLS CUI 2011AA)
260676000 (SNOMED CT 2011_0131)
C0003211 (UMLS CUI 2011AA)
16403005 (SNOMED CT 2011_0131)
C0332257 (UMLS CUI 2011AA)
55919000 (SNOMED CT 2011_0131)
C1257954 (UMLS CUI 2011AA)
387050005 (SNOMED CT 2011_0131)
Pregnancy or lactation. Women of childbearing potential must maintain effective contraception during the study period as judged by the investigator.
Item
Pregnancy or lactation. Women of childbearing potential must maintain effective contraception during the study period as judged by the investigator.
boolean
C0032961 (UMLS CUI 2011AA)
289908002 (SNOMED CT 2011_0131)
10036556 (MedDRA 14.1)
MTHU035048 (LOINC Version 232)
C0006147 (UMLS CUI 2011AA)
10006247 (MedDRA 14.1)
C0043210 (UMLS CUI 2011AA)
224526002 (SNOMED CT 2011_0131)
C1148523 (UMLS CUI 2011AA)
C0237399 (UMLS CUI 2011AA)
C0024501 (UMLS CUI 2011AA)
C1704419 (UMLS CUI 2011AA)
254648000 (SNOMED CT 2011_0131)
C0700589 (UMLS CUI 2011AA)
146680009 (SNOMED CT 2011_0131)
10010808 (MedDRA 14.1)
C0347984 (UMLS CUI 2011AA)
371881003 (SNOMED CT 2011_0131)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
C1948053 (UMLS CUI 2011AA)
C0022423 (UMLS CUI 2011AA)
61254005 (SNOMED CT 2011_0131)
CL102947 (UMLS CUI 2011AA)
Need for continuous concomitant therapy with: (Anticoagulants, Corticosteroids at doses higher than explained under inclusion criterion)
Item
Need for continuous concomitant therapy with: (Anticoagulants, Corticosteroids at doses higher than explained under inclusion criterion)
boolean
C0686904 (UMLS CUI 2011AA)
103325001 (SNOMED CT 2011_0131)
C0549178 (UMLS CUI 2011AA)
C1707479 (UMLS CUI 2011AA)
C0003280 (UMLS CUI 2011AA)
372862008 (SNOMED CT 2011_0131)
C0001617 (UMLS CUI 2011AA)
79440004 (SNOMED CT 2011_0131)
C0178602 (UMLS CUI 2011AA)
260911001 (SNOMED CT 2011_0131)
C0444956 (UMLS CUI 2011AA)
261829003 (SNOMED CT 2011_0131)
C0681841 (UMLS CUI 2011AA)
MTHU013812 (LOINC Version 232)
CL425202 (UMLS CUI 2011AA)

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