ID

37607

Descripción

Is Endothelial Function a Predictor of Successful Ablation Therapy Provided to Patients With Atrial Fibrillation?; ODM derived from: https://clinicaltrials.gov/show/NCT02129842

Link

https://clinicaltrials.gov/show/NCT02129842

Palabras clave

Versiones (1)
  1. 11/8/19 11/8/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

11 de agosto de 2019

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.

Volver a los comentarios del modelo
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 Atrial Fibrillation NCT02129842

Inglés

Eligibility Atrial Fibrillation NCT02129842

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
all patients with af considered eligible for ablation treatment may be included in this study (following unsuccessful attempts with aad).
Descripción

Atrial Fibrillation Eligible Ablation | Anti-Arrhythmia Agents Unsuccessful

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C1548635
UMLS CUI [1,3]
C0547070
UMLS CUI [2,1]
C0003195
UMLS CUI [2,2]
C1272705
patients on optimal anticoagulation therapy
Descripción

Anticoagulation Therapy Optimal

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0003281
UMLS CUI [1,2]
C2698651
the minimum af documentation required as defined by the heart rhythm society
Descripción

Atrial Fibrillation Documentation Minimum

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0920316
UMLS CUI [1,3]
C1524031
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients age below 18 years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
cases with extremely abnormal anatomy (i.e., inverted heart)
Descripción

Anatomy Abnormal Extremely | Heart Inverted

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0700276
UMLS CUI [1,2]
C0205161
UMLS CUI [1,3]
C0205403
UMLS CUI [2,1]
C0018787
UMLS CUI [2,2]
C2349984
moderate or severe mitral valve disease or mitral prosthetic valve
Descripción

Disease of mitral valve Moderate | Disease of mitral valve Severe | Mitral valve prosthesis

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0026265
UMLS CUI [1,2]
C0205081
UMLS CUI [2,1]
C0026265
UMLS CUI [2,2]
C0205082
UMLS CUI [3]
C0182494
ejection fraction less than 30%
Descripción

Cardiac ejection fraction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232174
left atrial anteroposterior diameter more than 50 mm evaluated by echo or ct data (up to 6 months old)..
Descripción

Left atrium Diameter Antero-posterior | Evaluation Echocardiography | Evaluation CT Data

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0225860
UMLS CUI [1,2]
C1301886
UMLS CUI [1,3]
C0442212
UMLS CUI [2,1]
C1261322
UMLS CUI [2,2]
C0013516
UMLS CUI [3,1]
C1261322
UMLS CUI [3,2]
C0040405
UMLS CUI [3,3]
C1511726
previous atrial fibrillation ablation occurred less than 6 months prior
Descripción

Catheter ablation for atrial fibrillation Previous

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2702800
UMLS CUI [1,2]
C0205156
left atrium thrombus
Descripción

Thrombus of left atrium

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3532827
acute infective disease or sepsis in the last 3 months
Descripción

Communicable Disease | Sepsis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0243026
acute myocardial infarction in last 3 months
Descripción

Myocardial Infarction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027051
reduced expectancy of life (less than 12 months)
Descripción

Reduced life expectancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1858274
patient participating in another clinical study that investigates a drug or device unless prior approval is given by the sponsor
Descripción

Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
UMLS CUI [3]
C2346570
psychologically unstable patient or denies to give informed consent
Descripción

Unstable status Psychological | Informed Consent Refused

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0443343
UMLS CUI [1,2]
C0205486
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1705116
deformities of the digits of the upper extremities, which preclude adequate signal acquisition
Descripción

Fingers Deformity

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0016129
UMLS CUI [1,2]
C0302142
patients under the effect of short-acting nitroglycerin (3 hours washout period)
Descripción

Nitroglycerin Active short-term | Washout Period Duration

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0017887
UMLS CUI [1,2]
C0205177
UMLS CUI [1,3]
C0443303
UMLS CUI [2,1]
C1710661
UMLS CUI [2,2]
C0449238
patient suffering from a medical condition prohibiting blood flow occlusion in both arms
Descripción

Medical condition | Blood flow Occlusion Arm Restricted

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3843040
UMLS CUI [2,1]
C0232338
UMLS CUI [2,2]
C1947917
UMLS CUI [2,3]
C1140618
UMLS CUI [2,4]
C0443288
Volver a la parte superior de la página

Similar models

Eligibility Atrial Fibrillation NCT02129842

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Atrial Fibrillation Eligible Ablation | Anti-Arrhythmia Agents Unsuccessful
Item
all patients with af considered eligible for ablation treatment may be included in this study (following unsuccessful attempts with aad).
boolean
C0004238 (UMLS CUI [1,1])
C1548635 (UMLS CUI [1,2])
C0547070 (UMLS CUI [1,3])
C0003195 (UMLS CUI [2,1])
C1272705 (UMLS CUI [2,2])
Anticoagulation Therapy Optimal
Item
patients on optimal anticoagulation therapy
boolean
C0003281 (UMLS CUI [1,1])
C2698651 (UMLS CUI [1,2])
Atrial Fibrillation Documentation Minimum
Item
the minimum af documentation required as defined by the heart rhythm society
boolean
C0004238 (UMLS CUI [1,1])
C0920316 (UMLS CUI [1,2])
C1524031 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Age
Item
patients age below 18 years
boolean
C0001779 (UMLS CUI [1])
Anatomy Abnormal Extremely | Heart Inverted
Item
cases with extremely abnormal anatomy (i.e., inverted heart)
boolean
C0700276 (UMLS CUI [1,1])
C0205161 (UMLS CUI [1,2])
C0205403 (UMLS CUI [1,3])
C0018787 (UMLS CUI [2,1])
C2349984 (UMLS CUI [2,2])
Disease of mitral valve Moderate | Disease of mitral valve Severe | Mitral valve prosthesis
Item
moderate or severe mitral valve disease or mitral prosthetic valve
boolean
C0026265 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
C0026265 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0182494 (UMLS CUI [3])
Cardiac ejection fraction
Item
ejection fraction less than 30%
boolean
C0232174 (UMLS CUI [1])
Left atrium Diameter Antero-posterior | Evaluation Echocardiography | Evaluation CT Data
Item
left atrial anteroposterior diameter more than 50 mm evaluated by echo or ct data (up to 6 months old)..
boolean
C0225860 (UMLS CUI [1,1])
C1301886 (UMLS CUI [1,2])
C0442212 (UMLS CUI [1,3])
C1261322 (UMLS CUI [2,1])
C0013516 (UMLS CUI [2,2])
C1261322 (UMLS CUI [3,1])
C0040405 (UMLS CUI [3,2])
C1511726 (UMLS CUI [3,3])
Catheter ablation for atrial fibrillation Previous
Item
previous atrial fibrillation ablation occurred less than 6 months prior
boolean
C2702800 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
Thrombus of left atrium
Item
left atrium thrombus
boolean
C3532827 (UMLS CUI [1])
Communicable Disease | Sepsis
Item
acute infective disease or sepsis in the last 3 months
boolean
C0009450 (UMLS CUI [1])
C0243026 (UMLS CUI [2])
Myocardial Infarction
Item
acute myocardial infarction in last 3 months
boolean
C0027051 (UMLS CUI [1])
Reduced life expectancy
Item
reduced expectancy of life (less than 12 months)
boolean
C1858274 (UMLS CUI [1])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
patient participating in another clinical study that investigates a drug or device unless prior approval is given by the sponsor
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
Unstable status Psychological | Informed Consent Refused
Item
psychologically unstable patient or denies to give informed consent
boolean
C0443343 (UMLS CUI [1,1])
C0205486 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
Fingers Deformity
Item
deformities of the digits of the upper extremities, which preclude adequate signal acquisition
boolean
C0016129 (UMLS CUI [1,1])
C0302142 (UMLS CUI [1,2])
Nitroglycerin Active short-term | Washout Period Duration
Item
patients under the effect of short-acting nitroglycerin (3 hours washout period)
boolean
C0017887 (UMLS CUI [1,1])
C0205177 (UMLS CUI [1,2])
C0443303 (UMLS CUI [1,3])
C1710661 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
Medical condition | Blood flow Occlusion Arm Restricted
Item
patient suffering from a medical condition prohibiting blood flow occlusion in both arms
boolean
C3843040 (UMLS CUI [1])
C0232338 (UMLS CUI [2,1])
C1947917 (UMLS CUI [2,2])
C1140618 (UMLS CUI [2,3])
C0443288 (UMLS CUI [2,4])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

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