ID

21531

Descripción

NEXUS Study for the Treatment of de Novo Native Coronary Artery Lesions; ODM derived from: https://clinicaltrials.gov/show/NCT00231283

Link

https://clinicaltrials.gov/show/NCT00231283

Palabras clave

  1. 26/4/17 26/4/17 -
Subido en

26 de abril de 2017

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0

Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Coronary Artery Disease NCT00231283

Eligibility Coronary Artery Disease NCT00231283

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. male or non-pregnant female patients 18 years of age
Descripción

ID.1

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
2. diagnosis of angina pectoris as defined by canadian cardiovascular society classification (ccs i, ii, iii, iv) or unstable angina pectoris (braunwald classification b&c, i-ii) or patients with documented silent ischemia;
Descripción

ID.2

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0002962
UMLS CUI [1,2]
C0340291
UMLS CUI [1,3]
C1277207
3. treatment of a single de novo target lesion in a major native coronary artery;
Descripción

ID.3

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0205042
4. target lesion is 2.5 mm and 3.5 mm in diameter (visual estimate);
Descripción

ID.4

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1301886
UMLS CUI [1,2]
C0221198
5. target lesion is 30mm in length (visual estimate);
Descripción

ID.5

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1444754
6. target lesion stenosis is > 50% and < 100% (visual estimate);
Descripción

ID.6

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1261287
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. patient has experienced a q-wave or non-q-wave myocardial infarction with documented total ck > 2 times normal within the preceding 24 hours and the ck and ck-mb enzymes remain above normal at the time of treatment;
Descripción

ID.7

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0542269
UMLS CUI [1,2]
C0582803
UMLS CUI [1,3]
C0201973
2. has unstable angina classified as braunwald iii b or c, or is having a peri-infarction angina;
Descripción

ID.8

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0002965
3. significant (> 50%) stenoses proximal or distal to the target lesion that might require revascularization or impede runoff;
Descripción

ID.9

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1261287
UMLS CUI [1,2]
C0581603
4. documented left ventricular ejection fraction 25%;
Descripción

ID.10

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0428772
5. totally occluded vessel (timi 0 level);
Descripción

ID.11

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0429885
6. impaired renal function (creatinine > 3.0 mg/dl) at the time of treatment;
Descripción

ID.12

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0201975
UMLS CUI [1,2]
C0232807

Similar models

Eligibility Coronary Artery Disease NCT00231283

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
1. male or non-pregnant female patients 18 years of age
boolean
C0001779 (UMLS CUI [1])
ID.2
Item
2. diagnosis of angina pectoris as defined by canadian cardiovascular society classification (ccs i, ii, iii, iv) or unstable angina pectoris (braunwald classification b&c, i-ii) or patients with documented silent ischemia;
boolean
C0002962 (UMLS CUI [1,1])
C0340291 (UMLS CUI [1,2])
C1277207 (UMLS CUI [1,3])
ID.3
Item
3. treatment of a single de novo target lesion in a major native coronary artery;
boolean
C0087111 (UMLS CUI [1,1])
C0205042 (UMLS CUI [1,2])
ID.4
Item
4. target lesion is 2.5 mm and 3.5 mm in diameter (visual estimate);
boolean
C1301886 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
ID.5
Item
5. target lesion is 30mm in length (visual estimate);
boolean
C0221198 (UMLS CUI [1,1])
C1444754 (UMLS CUI [1,2])
ID.6
Item
6. target lesion stenosis is > 50% and < 100% (visual estimate);
boolean
C1261287 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.7
Item
1. patient has experienced a q-wave or non-q-wave myocardial infarction with documented total ck > 2 times normal within the preceding 24 hours and the ck and ck-mb enzymes remain above normal at the time of treatment;
boolean
C0542269 (UMLS CUI [1,1])
C0582803 (UMLS CUI [1,2])
C0201973 (UMLS CUI [1,3])
ID.8
Item
2. has unstable angina classified as braunwald iii b or c, or is having a peri-infarction angina;
boolean
C0002965 (UMLS CUI [1])
ID.9
Item
3. significant (> 50%) stenoses proximal or distal to the target lesion that might require revascularization or impede runoff;
boolean
C1261287 (UMLS CUI [1,1])
C0581603 (UMLS CUI [1,2])
ID.10
Item
4. documented left ventricular ejection fraction 25%;
boolean
C0428772 (UMLS CUI [1])
ID.11
Item
5. totally occluded vessel (timi 0 level);
boolean
C0429885 (UMLS CUI [1])
ID.12
Item
6. impaired renal function (creatinine > 3.0 mg/dl) at the time of treatment;
boolean
C0201975 (UMLS CUI [1,1])
C0232807 (UMLS CUI [1,2])

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

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