ID

4570

Descrição

ODM derived from http://clinicaltrials.gov/show/NCT00327379

Link

http://clinicaltrials.gov/show/NCT00327379

Palavras-chave

  1. 11/12/2013 11/12/2013 - Martin Dugas
  2. 17/09/2021 17/09/2021 -
Transferido a

11 de dezembro de 2013

DOI

Para um pedido faça login.

Licença

Creative Commons BY 4.0

Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Eligibility NCT00327379 Postoperative Hemorrhage

  1. StudyEvent: Eligibility
    1. Eligibility
Einschlusskriterien
Descrição

Einschlusskriterien

Alias
UMLS CUI 2011AA
CL425202
Alter >=18 Jahre
Descrição

age >=18 Years

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C0001779
SNOMED CT 2011_0131
397669002
Subjects requiring elective spinal fusion surgery involving 3 to 7 vertebral levels with instrumentation. One vertebral level is defined as encompassing two vertebral bodies and one inter-vertebral disc space, so that a contiguous spinal fusion involving 3 vertebral levels would include 4 vertebral bodies and 3 inter-vertebral disc spaces.
Descrição

Subjects requiring elective spinal fusion surgery involving 3 to 7 vertebral levels with instrumentation. One vertebral level is defined as encompassing two vertebral bodies and one inter-vertebral disc space, so that a contiguous spinal fusion involving 3 vertebral levels would include 4 vertebral bodies and 3 inter-vertebral disc spaces.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C0206058
SNOMED CT 2011_0131
274075007
MedDRA 14.1
10058829
UMLS CUI 2011AA
C0919636
MedDRA 14.1
10050505
UMLS CUI 2011AA
C0446409
SNOMED CT 2011_0131
263276005
UMLS CUI 2011AA
CL414307
UMLS CUI 2011AA
C0223084
SNOMED CT 2011_0131
3572006
UMLS CUI 2011AA
C1279061
SNOMED CT 2011_0131
181817002
UMLS CUI 2011AA
C1556138
UMLS CUI 2011AA
C0223088
SNOMED CT 2011_0131
47886009
Ausschlusskriterien
Descrição

Ausschlusskriterien

Alias
UMLS CUI 2011AA
CL425201
Subjects with previous exposure to aprotinin in the last 6 months. If the subject has undergone cardiac surgery in the last 6 months, all attempts should be made to ascertain if aprotinin was administered during cardiac surgery. If no records are available, or if the subject received aprotinin, the subject should be excluded.
Descrição

Subjects with previous exposure to aprotinin in the last 6 months. If the subject has undergone cardiac surgery in the last 6 months, all attempts should be made to ascertain if aprotinin was administered during cardiac surgery. If no records are available, or if the subject received aprotinin, the subject should be excluded.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C0205156
SNOMED CT 2011_0131
9130008
UMLS CUI 2011AA
C0332157
SNOMED CT 2011_0131
24932003
UMLS CUI 2011AA
C0592198
SNOMED CT 2011_0131
386961008
UMLS CUI 2011AA
C0018821
SNOMED CT 2011_0131
64915003
MedDRA 14.1
10061026
UMLS CUI 2011AA
C1521801
UMLS CUI 2011AA
C0347984
SNOMED CT 2011_0131
371881003
UMLS CUI 2011AA
C0034869
UMLS CUI 2011AA
CL411789
Subjects with a known or suspected allergy to aprotinin.
Descrição

Subjects with a known or suspected allergy to aprotinin.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C0205309
SNOMED CT 2011_0131
36692007
UMLS CUI 2011AA
C0750491
SNOMED CT 2011_0131
415684004
UMLS CUI 2011AA
C0020517
SNOMED CT 2011_0131
257550005
ICD-10-CM Version 2010
T78.40
UMLS CUI 2011AA
C0592198
SNOMED CT 2011_0131
386961008
UMLS CUI 2011AA
C0011900
SNOMED CT 2011_0131
439401001
LOINC Version 232
MTHU008876
Subjects with sepsis or a known bone infection.
Descrição

Subjects with sepsis or a known bone infection.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C0243026
SNOMED CT 2011_0131
91302008
MedDRA 14.1
10040047
ICD-9-CM Version 2011
995.91
UMLS CUI 2011AA
C0205309
SNOMED CT 2011_0131
36692007
UMLS CUI 2011AA
C2242472
SNOMED CT 2011_0131
111253001
ICD-10-CM Version 2010
M86.9
ICD-9-CM Version 2011
730.9
CTCAE 1105E
E11314
Personal history of malignant neoplasm of bone
Descrição

Subjects with known bone malignancy.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C0260447
ICD-10-CM Version 2010
Z85.830
ICD-9-CM Version 2011
V10.81
Subjects with a creatinine clearance <30mL/min as calculated by the Cockcroft-Gault formula.
Descrição

Subjects with a creatinine clearance <30mL/min as calculated by the Cockcroft-Gault formula.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C2711451
SNOMED CT 2011_0131
442407001
UMLS CUI 2011AA
C0444686
SNOMED CT 2011_0131
258090004
Subjects with a history of bleeding diathesis or known coagulation factor deficiency.
Descrição

Subjects with a history of bleeding diathesis or known coagulation factor deficiency.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
CL421546
SNOMED CT 2011_0131
392521001
UMLS CUI 2011AA
C1458140
SNOMED CT 2011_0131
248250000
MedDRA 14.1
10005134
UMLS CUI 2011AA
C0205309
SNOMED CT 2011_0131
36692007
UMLS CUI 2011AA
C0849773
SNOMED CT 2011_0131
86075001
MedDRA 14.1
10067787
ICD-9-CM Version 2011
286
Subjects with failure of a major organ system or any active significant medical illness that in the opinion of the Investigator is likely to affect the subject's ability to complete the study or precludes the subject's participation in the study.
Descrição

Subjects with failure of a major organ system or any active significant medical illness that in the opinion of the Investigator is likely to affect the subject's ability to complete the study or precludes the subject's participation in the study.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C0231174
SNOMED CT 2011_0131
76797004
UMLS CUI 2011AA
C0205164
SNOMED CT 2011_0131
255603008
UMLS CUI 2011AA
C0460002
SNOMED CT 2011_0131
91689009
UMLS CUI 2011AA
C0205177
SNOMED CT 2011_0131
55561003
UMLS CUI 2011AA
C0750502
SNOMED CT 2011_0131
386134007
UMLS CUI 2011AA
C0205476
SNOMED CT 2011_0131
74188005
UMLS CUI 2011AA
C0221423
SNOMED CT 2011_0131
39104002
MedDRA 14.1
10040658
ICD-10-CM Version 2010
R69
UMLS CUI 2011AA
C0085732
SNOMED CT 2011_0131
371150009
UMLS CUI 2011AA
C0205197
SNOMED CT 2011_0131
255594003
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008
UMLS CUI 2011AA
C2348568
Subjects who refuse to receive allogenic blood products for religious or other reasons.
Descrição

Subjects who refuse to receive allogenic blood products for religious or other reasons.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C1411169
UMLS CUI 2011AA
CL428796
MedDRA 14.1
10071089
Subjects whose preoperative red blood cell volume is so low that a blood transfusion would be likely to be given perioperatively (preoperative hematocrit or hemoglobin values <24% or <8 g/dl, respectively).
Descrição

Subjects whose preoperative red blood cell volume is so low that a blood transfusion would be likely to be given perioperatively (preoperative hematocrit or hemoglobin values <24% or <8 g/dl, respectively).

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C0445204
SNOMED CT 2011_0131
262068006
UMLS CUI 2011AA
C2711689
SNOMED CT 2011_0131
441791009
UMLS CUI 2011AA
C0005841
SNOMED CT 2011_0131
116859006
MedDRA 14.1
10005835
LOINC Version 232
MTHU020992
UMLS CUI 2011AA
C1518988
UMLS CUI 2011AA
C0744727
MedDRA 14.1
10018838
ICD-10-CM Version 2010
R71.0
UMLS CUI 2011AA
C0162119
SNOMED CT 2011_0131
165397008
MedDRA 14.1
10018884
Subjects who have participated in an investigational drug study within the past 30 days.
Descrição

Subjects who have participated in an investigational drug study within the past 30 days.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C2348568
HL7 V3 2006_05
PART
UMLS CUI 2011AA
C0013230
Subjects with a history of deep vein thrombosis or pulmonary embolism.
Descrição

Subjects with a history of deep vein thrombosis or pulmonary embolism.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
CL421546
SNOMED CT 2011_0131
392521001
UMLS CUI 2011AA
C0149871
SNOMED CT 2011_0131
128053003
MedDRA 14.1
10051055
ICD-10-CM Version 2010
I82.40
UMLS CUI 2011AA
C0034065
SNOMED CT 2011_0131
59282003
MedDRA 14.1
10037377
ICD-10-CM Version 2010
I26
ICD-9-CM Version 2011
415.1
Subjects who are pregnant or breast feeding.
Descrição

Subjects who are pregnant or breast feeding.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C0549206
MedDRA 14.1
10036586
UMLS CUI 2011AA
C0006147
MedDRA 14.1
10006247
Women of childbearing potential in whom the possibility of pregnancy cannot be excluded by a negative serum pregnancy test at screening.
Descrição

Women of childbearing potential in whom the possibility of pregnancy cannot be excluded by a negative serum pregnancy test at screening.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C0043210
SNOMED CT 2011_0131
224526002
UMLS CUI 2011AA
C1148523
UMLS CUI 2011AA
C0237399
UMLS CUI 2011AA
C0332149
SNOMED CT 2011_0131
371930009
UMLS CUI 2011AA
CL425201
UMLS CUI 2011AA
C0430061
SNOMED CT 2011_0131
166435006
UMLS CUI 2011AA
C1409616
Women of childbearing potential who are not using a reliable method of contraception.
Descrição

Women of childbearing potential who are not using a reliable method of contraception.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C0043210
SNOMED CT 2011_0131
224526002
UMLS CUI 2011AA
C1148523
UMLS CUI 2011AA
C0237399
UMLS CUI 2011AA
C0700589
SNOMED CT 2011_0131
146680009
MedDRA 14.1
10010808
Antifibrinolytikum
Descrição

Planned use of other antifibrinolytic agents.

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C0003304
SNOMED CT 2011_0131
75064004
Subjects on chronic anticoagulant treatment with Vit K antagonists that cannot be temporarily discontinued for the surgical procedure (as per local practices).
Descrição

Subjects on chronic anticoagulant treatment with Vit K antagonists that cannot be temporarily discontinued for the surgical procedure (as per local practices).

Tipo de dados

boolean

Alias
UMLS CUI 2011AA
C0205191
SNOMED CT 2011_0131
90734009
UMLS CUI 2011AA
C0150457
SNOMED CT 2011_0131
182764009
MedDRA 14.1
10053468
UMLS CUI 2011AA
C1096489
MedDRA 14.1
10053755
UMLS CUI 2011AA
C0205374
SNOMED CT 2011_0131
14803004
UMLS CUI 2011AA
C1444662
SNOMED CT 2011_0131
410546004
UMLS CUI 2011AA
C0543467
SNOMED CT 2011_0131
83578000
MedDRA 14.1
10051332
LOINC Version 232
MTHU000079
UMLS CUI 2011AA
CL415116
UMLS CUI 2011AA
C0032893

Similar models

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Einschlusskriterien
CL425202 (UMLS CUI 2011AA)
age >=18 Years
Item
Alter >=18 Jahre
boolean
C0001779 (UMLS CUI 2011AA)
397669002 (SNOMED CT 2011_0131)
Subjects requiring elective spinal fusion surgery involving 3 to 7 vertebral levels with instrumentation. One vertebral level is defined as encompassing two vertebral bodies and one inter-vertebral disc space, so that a contiguous spinal fusion involving 3 vertebral levels would include 4 vertebral bodies and 3 inter-vertebral disc spaces.
Item
Subjects requiring elective spinal fusion surgery involving 3 to 7 vertebral levels with instrumentation. One vertebral level is defined as encompassing two vertebral bodies and one inter-vertebral disc space, so that a contiguous spinal fusion involving 3 vertebral levels would include 4 vertebral bodies and 3 inter-vertebral disc spaces.
boolean
C0206058 (UMLS CUI 2011AA)
274075007 (SNOMED CT 2011_0131)
10058829 (MedDRA 14.1)
C0919636 (UMLS CUI 2011AA)
10050505 (MedDRA 14.1)
C0446409 (UMLS CUI 2011AA)
263276005 (SNOMED CT 2011_0131)
CL414307 (UMLS CUI 2011AA)
C0223084 (UMLS CUI 2011AA)
3572006 (SNOMED CT 2011_0131)
C1279061 (UMLS CUI 2011AA)
181817002 (SNOMED CT 2011_0131)
C1556138 (UMLS CUI 2011AA)
C0223088 (UMLS CUI 2011AA)
47886009 (SNOMED CT 2011_0131)
Item Group
Ausschlusskriterien
CL425201 (UMLS CUI 2011AA)
Subjects with previous exposure to aprotinin in the last 6 months. If the subject has undergone cardiac surgery in the last 6 months, all attempts should be made to ascertain if aprotinin was administered during cardiac surgery. If no records are available, or if the subject received aprotinin, the subject should be excluded.
Item
Subjects with previous exposure to aprotinin in the last 6 months. If the subject has undergone cardiac surgery in the last 6 months, all attempts should be made to ascertain if aprotinin was administered during cardiac surgery. If no records are available, or if the subject received aprotinin, the subject should be excluded.
boolean
C0205156 (UMLS CUI 2011AA)
9130008 (SNOMED CT 2011_0131)
C0332157 (UMLS CUI 2011AA)
24932003 (SNOMED CT 2011_0131)
C0592198 (UMLS CUI 2011AA)
386961008 (SNOMED CT 2011_0131)
C0018821 (UMLS CUI 2011AA)
64915003 (SNOMED CT 2011_0131)
10061026 (MedDRA 14.1)
C1521801 (UMLS CUI 2011AA)
C0347984 (UMLS CUI 2011AA)
371881003 (SNOMED CT 2011_0131)
C0034869 (UMLS CUI 2011AA)
CL411789 (UMLS CUI 2011AA)
Subjects with a known or suspected allergy to aprotinin.
Item
Subjects with a known or suspected allergy to aprotinin.
boolean
C0205309 (UMLS CUI 2011AA)
36692007 (SNOMED CT 2011_0131)
C0750491 (UMLS CUI 2011AA)
415684004 (SNOMED CT 2011_0131)
C0020517 (UMLS CUI 2011AA)
257550005 (SNOMED CT 2011_0131)
T78.40 (ICD-10-CM Version 2010)
C0592198 (UMLS CUI 2011AA)
386961008 (SNOMED CT 2011_0131)
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
Subjects with sepsis or a known bone infection.
Item
Subjects with sepsis or a known bone infection.
boolean
C0243026 (UMLS CUI 2011AA)
91302008 (SNOMED CT 2011_0131)
10040047 (MedDRA 14.1)
995.91 (ICD-9-CM Version 2011)
C0205309 (UMLS CUI 2011AA)
36692007 (SNOMED CT 2011_0131)
C2242472 (UMLS CUI 2011AA)
111253001 (SNOMED CT 2011_0131)
M86.9 (ICD-10-CM Version 2010)
730.9 (ICD-9-CM Version 2011)
E11314 (CTCAE 1105E)
Subjects with known bone malignancy.
Item
Personal history of malignant neoplasm of bone
boolean
C0260447 (UMLS CUI 2011AA)
Z85.830 (ICD-10-CM Version 2010)
V10.81 (ICD-9-CM Version 2011)
Subjects with a creatinine clearance <30mL/min as calculated by the Cockcroft-Gault formula.
Item
Subjects with a creatinine clearance <30mL/min as calculated by the Cockcroft-Gault formula.
boolean
C2711451 (UMLS CUI 2011AA)
442407001 (SNOMED CT 2011_0131)
C0444686 (UMLS CUI 2011AA)
258090004 (SNOMED CT 2011_0131)
Subjects with a history of bleeding diathesis or known coagulation factor deficiency.
Item
Subjects with a history of bleeding diathesis or known coagulation factor deficiency.
boolean
CL421546 (UMLS CUI 2011AA)
392521001 (SNOMED CT 2011_0131)
C1458140 (UMLS CUI 2011AA)
248250000 (SNOMED CT 2011_0131)
10005134 (MedDRA 14.1)
C0205309 (UMLS CUI 2011AA)
36692007 (SNOMED CT 2011_0131)
C0849773 (UMLS CUI 2011AA)
86075001 (SNOMED CT 2011_0131)
10067787 (MedDRA 14.1)
286 (ICD-9-CM Version 2011)
Subjects with failure of a major organ system or any active significant medical illness that in the opinion of the Investigator is likely to affect the subject's ability to complete the study or precludes the subject's participation in the study.
Item
Subjects with failure of a major organ system or any active significant medical illness that in the opinion of the Investigator is likely to affect the subject's ability to complete the study or precludes the subject's participation in the study.
boolean
C0231174 (UMLS CUI 2011AA)
76797004 (SNOMED CT 2011_0131)
C0205164 (UMLS CUI 2011AA)
255603008 (SNOMED CT 2011_0131)
C0460002 (UMLS CUI 2011AA)
91689009 (SNOMED CT 2011_0131)
C0205177 (UMLS CUI 2011AA)
55561003 (SNOMED CT 2011_0131)
C0750502 (UMLS CUI 2011AA)
386134007 (SNOMED CT 2011_0131)
C0205476 (UMLS CUI 2011AA)
74188005 (SNOMED CT 2011_0131)
C0221423 (UMLS CUI 2011AA)
39104002 (SNOMED CT 2011_0131)
10040658 (MedDRA 14.1)
R69 (ICD-10-CM Version 2010)
C0085732 (UMLS CUI 2011AA)
371150009 (SNOMED CT 2011_0131)
C0205197 (UMLS CUI 2011AA)
255594003 (SNOMED CT 2011_0131)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
C2348568 (UMLS CUI 2011AA)
Subjects who refuse to receive allogenic blood products for religious or other reasons.
Item
Subjects who refuse to receive allogenic blood products for religious or other reasons.
boolean
C1411169 (UMLS CUI 2011AA)
CL428796 (UMLS CUI 2011AA)
10071089 (MedDRA 14.1)
Subjects whose preoperative red blood cell volume is so low that a blood transfusion would be likely to be given perioperatively (preoperative hematocrit or hemoglobin values <24% or <8 g/dl, respectively).
Item
Subjects whose preoperative red blood cell volume is so low that a blood transfusion would be likely to be given perioperatively (preoperative hematocrit or hemoglobin values <24% or <8 g/dl, respectively).
boolean
C0445204 (UMLS CUI 2011AA)
262068006 (SNOMED CT 2011_0131)
C2711689 (UMLS CUI 2011AA)
441791009 (SNOMED CT 2011_0131)
C0005841 (UMLS CUI 2011AA)
116859006 (SNOMED CT 2011_0131)
10005835 (MedDRA 14.1)
MTHU020992 (LOINC Version 232)
C1518988 (UMLS CUI 2011AA)
C0744727 (UMLS CUI 2011AA)
10018838 (MedDRA 14.1)
R71.0 (ICD-10-CM Version 2010)
C0162119 (UMLS CUI 2011AA)
165397008 (SNOMED CT 2011_0131)
10018884 (MedDRA 14.1)
Subjects who have participated in an investigational drug study within the past 30 days.
Item
Subjects who have participated in an investigational drug study within the past 30 days.
boolean
C2348568 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
C0013230 (UMLS CUI 2011AA)
Subjects with a history of deep vein thrombosis or pulmonary embolism.
Item
Subjects with a history of deep vein thrombosis or pulmonary embolism.
boolean
CL421546 (UMLS CUI 2011AA)
392521001 (SNOMED CT 2011_0131)
C0149871 (UMLS CUI 2011AA)
128053003 (SNOMED CT 2011_0131)
10051055 (MedDRA 14.1)
I82.40 (ICD-10-CM Version 2010)
C0034065 (UMLS CUI 2011AA)
59282003 (SNOMED CT 2011_0131)
10037377 (MedDRA 14.1)
I26 (ICD-10-CM Version 2010)
415.1 (ICD-9-CM Version 2011)
Subjects who are pregnant or breast feeding.
Item
Subjects who are pregnant or breast feeding.
boolean
C0549206 (UMLS CUI 2011AA)
10036586 (MedDRA 14.1)
C0006147 (UMLS CUI 2011AA)
10006247 (MedDRA 14.1)
Women of childbearing potential in whom the possibility of pregnancy cannot be excluded by a negative serum pregnancy test at screening.
Item
Women of childbearing potential in whom the possibility of pregnancy cannot be excluded by a negative serum pregnancy test at screening.
boolean
C0043210 (UMLS CUI 2011AA)
224526002 (SNOMED CT 2011_0131)
C1148523 (UMLS CUI 2011AA)
C0237399 (UMLS CUI 2011AA)
C0332149 (UMLS CUI 2011AA)
371930009 (SNOMED CT 2011_0131)
CL425201 (UMLS CUI 2011AA)
C0430061 (UMLS CUI 2011AA)
166435006 (SNOMED CT 2011_0131)
C1409616 (UMLS CUI 2011AA)
Women of childbearing potential who are not using a reliable method of contraception.
Item
Women of childbearing potential who are not using a reliable method of contraception.
boolean
C0043210 (UMLS CUI 2011AA)
224526002 (SNOMED CT 2011_0131)
C1148523 (UMLS CUI 2011AA)
C0237399 (UMLS CUI 2011AA)
C0700589 (UMLS CUI 2011AA)
146680009 (SNOMED CT 2011_0131)
10010808 (MedDRA 14.1)
Planned use of other antifibrinolytic agents.
Item
Antifibrinolytikum
boolean
C0003304 (UMLS CUI 2011AA)
75064004 (SNOMED CT 2011_0131)
Subjects on chronic anticoagulant treatment with Vit K antagonists that cannot be temporarily discontinued for the surgical procedure (as per local practices).
Item
Subjects on chronic anticoagulant treatment with Vit K antagonists that cannot be temporarily discontinued for the surgical procedure (as per local practices).
boolean
C0205191 (UMLS CUI 2011AA)
90734009 (SNOMED CT 2011_0131)
C0150457 (UMLS CUI 2011AA)
182764009 (SNOMED CT 2011_0131)
10053468 (MedDRA 14.1)
C1096489 (UMLS CUI 2011AA)
10053755 (MedDRA 14.1)
C0205374 (UMLS CUI 2011AA)
14803004 (SNOMED CT 2011_0131)
C1444662 (UMLS CUI 2011AA)
410546004 (SNOMED CT 2011_0131)
C0543467 (UMLS CUI 2011AA)
83578000 (SNOMED CT 2011_0131)
10051332 (MedDRA 14.1)
MTHU000079 (LOINC Version 232)
CL415116 (UMLS CUI 2011AA)
C0032893 (UMLS CUI 2011AA)

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial