ID

28383

Descripción

Post Approval Registry of Corox OTW, Endocardial, Left Ventricular Steroid Lead, Bipolar; ODM derived from: https://clinicaltrials.gov/show/NCT00810264

Link

https://clinicaltrials.gov/show/NCT00810264

Palabras clave

Versiones (1)
  1. 9/1/18 9/1/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

9 de enero de 2018

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 Congestive Heart Failure NCT00810264

Inglés

Eligibility Congestive Heart Failure NCT00810264

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
successfully implanted biotronik crt system, including a corox bp lv lead, from 7-180 days prior to enrollment
Descripción

Cardiac Resynchronization Therapy Device Implantation Successful | Other Coding

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2936377
UMLS CUI [1,2]
C0021107
UMLS CUI [1,3]
C1272703
UMLS CUI [2]
C3846158
able to understand the nature of the registry and give informed consent
Descripción

Comprehension Enrollment | Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C1516879
UMLS CUI [2]
C0021430
available for follow-up visits on a regular basis at the investigational site
Descripción

Patient Available Follow-up visit

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0470187
UMLS CUI [1,3]
C0589121
age greater than or equal to 18 years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
enrolled in any ide clinical study
Descripción

Study Subject Participation Status | IDE Clinical Trial

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C2826366
UMLS CUI [2,2]
C0008976
planned cardiac surgical procedures or interventional measures within the next 6 months
Descripción

Cardiac Surgery procedures Planned | Interventional procedure Planned

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018821
UMLS CUI [1,2]
C1301732
UMLS CUI [2,1]
C0184661
UMLS CUI [2,2]
C1301732
expected to receive a heart transplant within 1 year
Descripción

Heart Transplantation Expected

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018823
UMLS CUI [1,2]
C1517001
life expectancy less than 1 year
Descripción

Life Expectancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023671
presence of another life-threatening, underlying illness separate from their cardiac disorder
Descripción

Comorbidity Life Threatening | Independent of Heart Disease

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C2826244
UMLS CUI [2,1]
C0332291
UMLS CUI [2,2]
C0018799
pregnancy
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
inability to provide date of implant, devices implanted, age, gender, and whether the patient experienced any protocol-defined adverse events since implant
Descripción

Protocol Compliance Unable | Implant Date No Information Available | Device implant No Information Available | Age No Information Available | Gender No Information Available | Adverse event No Information Available

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021107
UMLS CUI [2,2]
C0011008
UMLS CUI [2,3]
C1546437
UMLS CUI [3,1]
C0948629
UMLS CUI [3,2]
C1546437
UMLS CUI [4,1]
C0001779
UMLS CUI [4,2]
C1546437
UMLS CUI [5,1]
C0079399
UMLS CUI [5,2]
C1546437
UMLS CUI [6,1]
C0877248
UMLS CUI [6,2]
C1546437
Volver a la parte superior de la página

Similar models

Eligibility Congestive Heart Failure NCT00810264

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Cardiac Resynchronization Therapy Device Implantation Successful | Other Coding
Item
successfully implanted biotronik crt system, including a corox bp lv lead, from 7-180 days prior to enrollment
boolean
C2936377 (UMLS CUI [1,1])
C0021107 (UMLS CUI [1,2])
C1272703 (UMLS CUI [1,3])
C3846158 (UMLS CUI [2])
Comprehension Enrollment | Informed Consent
Item
able to understand the nature of the registry and give informed consent
boolean
C0162340 (UMLS CUI [1,1])
C1516879 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
Patient Available Follow-up visit
Item
available for follow-up visits on a regular basis at the investigational site
boolean
C0030705 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
C0589121 (UMLS CUI [1,3])
Age
Item
age greater than or equal to 18 years
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Study Subject Participation Status | IDE Clinical Trial
Item
enrolled in any ide clinical study
boolean
C2348568 (UMLS CUI [1])
C2826366 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
Cardiac Surgery procedures Planned | Interventional procedure Planned
Item
planned cardiac surgical procedures or interventional measures within the next 6 months
boolean
C0018821 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0184661 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Heart Transplantation Expected
Item
expected to receive a heart transplant within 1 year
boolean
C0018823 (UMLS CUI [1,1])
C1517001 (UMLS CUI [1,2])
Life Expectancy
Item
life expectancy less than 1 year
boolean
C0023671 (UMLS CUI [1])
Comorbidity Life Threatening | Independent of Heart Disease
Item
presence of another life-threatening, underlying illness separate from their cardiac disorder
boolean
C0009488 (UMLS CUI [1,1])
C2826244 (UMLS CUI [1,2])
C0332291 (UMLS CUI [2,1])
C0018799 (UMLS CUI [2,2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Protocol Compliance Unable | Implant Date No Information Available | Device implant No Information Available | Age No Information Available | Gender No Information Available | Adverse event No Information Available
Item
inability to provide date of implant, devices implanted, age, gender, and whether the patient experienced any protocol-defined adverse events since implant
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021107 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C1546437 (UMLS CUI [2,3])
C0948629 (UMLS CUI [3,1])
C1546437 (UMLS CUI [3,2])
C0001779 (UMLS CUI [4,1])
C1546437 (UMLS CUI [4,2])
C0079399 (UMLS CUI [5,1])
C1546437 (UMLS CUI [5,2])
C0877248 (UMLS CUI [6,1])
C1546437 (UMLS CUI [6,2])
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