ID

37525

Descripción

NAVISTAR® THERMOCOOL® SF Catheter: Observational Study; ODM derived from: https://clinicaltrials.gov/show/NCT01585961

Link

https://clinicaltrials.gov/show/NCT01585961

Palabras clave

Versiones (1)
  1. 5/8/19 5/8/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

5 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 NCT01585961

Inglés

Eligibility Atrial Fibrillation NCT01585961

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
drug refractory, recurrent, symptomatic paroxysmal atrial fibrillation
Descripción

Paroxysmal atrial fibrillation Symptomatic Recurrent | Paroxysmal atrial fibrillation Unresponsive to Pharmaceutical Preparations

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0235480
UMLS CUI [1,2]
C0231220
UMLS CUI [1,3]
C2945760
UMLS CUI [2,1]
C0235480
UMLS CUI [2,2]
C0205269
UMLS CUI [2,3]
C0013227
age 18 years or older
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
patients must be able and willing to provide written informed consent to participate in the study
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
atrial fibrillation secondary to electrolyte imbalance, thyroid disease, or reversible or non-cardiac cause
Descripción

Atrial Fibrillation Secondary to Electrolyte imbalance | Atrial Fibrillation Secondary to Thyroid Disease | Atrial Fibrillation Secondary to Cause Reversible | Atrial Fibrillation Secondary to Cause | Exception Cause cardiac

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0175668
UMLS CUI [1,3]
C0342579
UMLS CUI [2,1]
C0004238
UMLS CUI [2,2]
C0175668
UMLS CUI [2,3]
C0040128
UMLS CUI [3,1]
C0004238
UMLS CUI [3,2]
C0175668
UMLS CUI [3,3]
C0015127
UMLS CUI [3,4]
C0205343
UMLS CUI [4,1]
C0004238
UMLS CUI [4,2]
C0175668
UMLS CUI [4,3]
C0015127
UMLS CUI [5,1]
C1705847
UMLS CUI [5,2]
C0015127
UMLS CUI [5,3]
C0018787
previous ablation for atrial fibrillation
Descripción

Catheter ablation for atrial fibrillation Previous

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2702800
UMLS CUI [1,2]
C0205156
episodes of atrial fibrillation that last longer than 30 days and are terminated via cardioversion
Descripción

Atrial Fibrillation Episode Duration | Episode Ending Due to Electric Countershock

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0332189
UMLS CUI [1,3]
C0449238
UMLS CUI [2,1]
C0332189
UMLS CUI [2,2]
C2746065
UMLS CUI [2,3]
C0678226
UMLS CUI [2,4]
C0013778
uncontrolled heart failure, or nyha class iii or iv heart failure
Descripción

Heart failure Uncontrolled | Heart failure New York Heart Association Classification

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0205318
UMLS CUI [2,1]
C0018801
UMLS CUI [2,2]
C1275491
documented intra-atrial thrombus or other abnormality on pre-ablation echocardiogram
Descripción

Atrial thrombus | Abnormality Pre-ablation echocardiography

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0340517
UMLS CUI [2,1]
C1704258
UMLS CUI [2,2]
C2041213
contraindication to anticoagulation
Descripción

Medical contraindication Anticoagulation Therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0003281
stroke, cardiac surgery, unstable angina, myocardial infarction or percutaneous coronary intervention within the past 3 months
Descripción

Cerebrovascular accident | Cardiac Surgery | Angina, Unstable | Myocardial Infarction | Percutaneous Coronary Intervention

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038454
UMLS CUI [2]
C0018821
UMLS CUI [3]
C0002965
UMLS CUI [4]
C0027051
UMLS CUI [5]
C1532338
awaiting cardiac transplantation
Descripción

Heart Transplantation Expected

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018823
UMLS CUI [1,2]
C1517001
heart disease in which corrective surgery is anticipated within 6 months
Descripción

Heart Disease | Correction Surgical Anticipated

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0018799
UMLS CUI [2,1]
C1947976
UMLS CUI [2,2]
C0543467
UMLS CUI [2,3]
C3840775
enrollment in investigational drug, biologic or device study
Descripción

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

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
UMLS CUI [3]
C0005515
UMLS CUI [4]
C2346570
subjects unwilling to comply with protocol or follow-up requirements
Descripción

Protocol Compliance Unwilling

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C0558080
patients who are pregnant
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
Volver a la parte superior de la página

Similar models

Eligibility Atrial Fibrillation NCT01585961

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Paroxysmal atrial fibrillation Symptomatic Recurrent | Paroxysmal atrial fibrillation Unresponsive to Pharmaceutical Preparations
Item
drug refractory, recurrent, symptomatic paroxysmal atrial fibrillation
boolean
C0235480 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C2945760 (UMLS CUI [1,3])
C0235480 (UMLS CUI [2,1])
C0205269 (UMLS CUI [2,2])
C0013227 (UMLS CUI [2,3])
Age
Item
age 18 years or older
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
patients must be able and willing to provide written informed consent to participate in the study
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Atrial Fibrillation Secondary to Electrolyte imbalance | Atrial Fibrillation Secondary to Thyroid Disease | Atrial Fibrillation Secondary to Cause Reversible | Atrial Fibrillation Secondary to Cause | Exception Cause cardiac
Item
atrial fibrillation secondary to electrolyte imbalance, thyroid disease, or reversible or non-cardiac cause
boolean
C0004238 (UMLS CUI [1,1])
C0175668 (UMLS CUI [1,2])
C0342579 (UMLS CUI [1,3])
C0004238 (UMLS CUI [2,1])
C0175668 (UMLS CUI [2,2])
C0040128 (UMLS CUI [2,3])
C0004238 (UMLS CUI [3,1])
C0175668 (UMLS CUI [3,2])
C0015127 (UMLS CUI [3,3])
C0205343 (UMLS CUI [3,4])
C0004238 (UMLS CUI [4,1])
C0175668 (UMLS CUI [4,2])
C0015127 (UMLS CUI [4,3])
C1705847 (UMLS CUI [5,1])
C0015127 (UMLS CUI [5,2])
C0018787 (UMLS CUI [5,3])
Catheter ablation for atrial fibrillation Previous
Item
previous ablation for atrial fibrillation
boolean
C2702800 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
Atrial Fibrillation Episode Duration | Episode Ending Due to Electric Countershock
Item
episodes of atrial fibrillation that last longer than 30 days and are terminated via cardioversion
boolean
C0004238 (UMLS CUI [1,1])
C0332189 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
C0332189 (UMLS CUI [2,1])
C2746065 (UMLS CUI [2,2])
C0678226 (UMLS CUI [2,3])
C0013778 (UMLS CUI [2,4])
Heart failure Uncontrolled | Heart failure New York Heart Association Classification
Item
uncontrolled heart failure, or nyha class iii or iv heart failure
boolean
C0018801 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0018801 (UMLS CUI [2,1])
C1275491 (UMLS CUI [2,2])
Atrial thrombus | Abnormality Pre-ablation echocardiography
Item
documented intra-atrial thrombus or other abnormality on pre-ablation echocardiogram
boolean
C0340517 (UMLS CUI [1])
C1704258 (UMLS CUI [2,1])
C2041213 (UMLS CUI [2,2])
Medical contraindication Anticoagulation Therapy
Item
contraindication to anticoagulation
boolean
C1301624 (UMLS CUI [1,1])
C0003281 (UMLS CUI [1,2])
Cerebrovascular accident | Cardiac Surgery | Angina, Unstable | Myocardial Infarction | Percutaneous Coronary Intervention
Item
stroke, cardiac surgery, unstable angina, myocardial infarction or percutaneous coronary intervention within the past 3 months
boolean
C0038454 (UMLS CUI [1])
C0018821 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
C0027051 (UMLS CUI [4])
C1532338 (UMLS CUI [5])
Heart Transplantation Expected
Item
awaiting cardiac transplantation
boolean
C0018823 (UMLS CUI [1,1])
C1517001 (UMLS CUI [1,2])
Heart Disease | Correction Surgical Anticipated
Item
heart disease in which corrective surgery is anticipated within 6 months
boolean
C0018799 (UMLS CUI [1])
C1947976 (UMLS CUI [2,1])
C0543467 (UMLS CUI [2,2])
C3840775 (UMLS CUI [2,3])
Study Subject Participation Status | Investigational New Drugs | Biological Agents | Investigational Medical Device
Item
enrollment in investigational drug, biologic or device study
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C0005515 (UMLS CUI [3])
C2346570 (UMLS CUI [4])
Protocol Compliance Unwilling
Item
subjects unwilling to comply with protocol or follow-up requirements
boolean
C0525058 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
Pregnancy
Item
patients who are pregnant
boolean
C0032961 (UMLS CUI [1])
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