ID

29472

Descripción

Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT) Candidates; ODM derived from: https://clinicaltrials.gov/show/NCT00887237

Link

https://clinicaltrials.gov/show/NCT00887237

Palabras clave

Versiones (1)
  1. 29/3/18 29/3/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

29 de marzo 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 Heart Failure NCT00887237

Inglés

Eligibility Heart Failure NCT00887237

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
signed informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
> 18 years old
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
cardiac resynchronization indication : new york heart association (nyha) class iii/iv
Descripción

Indication Cardiac Resynchronization Therapy | New York Heart Association Classification

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C1167956
UMLS CUI [2]
C1275491
& qrs width > 120 ms milliseconds (ms) or nyha class ii & qrs width > 150 ms
Descripción

QRS complex duration | New York Heart Association Classification

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0429025
UMLS CUI [2]
C1275491
sinus rhythm
Descripción

Sinus rhythm

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232201
first implant procedure
Descripción

Implantation procedure First

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021107
UMLS CUI [1,2]
C0205435
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
permanent ventricular tachycardia
Descripción

Ventricular Tachycardia Permanent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0042514
UMLS CUI [1,2]
C0205355
permanent pacing indication for 3rd degree atrioventricular (av) block
Descripción

Indication Pacing Permanent | Complete atrioventricular block

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0199640
UMLS CUI [1,3]
C0205355
UMLS CUI [2]
C0151517
diagnosed or suspected acute myocarditis
Descripción

Myocarditis | Myocarditis Suspected

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027059
UMLS CUI [2,1]
C0027059
UMLS CUI [2,2]
C0750491
less than 1 year life expectancy related to a non-cardiovascular disease
Descripción

Life Expectancy Due to Disease | Exception Cardiovascular Diseases

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0023671
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0012634
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0007222
impossibility to perform follow-up in the investigative center
Descripción

Clinical Study Follow-up Perform Unsuccessful

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C0884358
UMLS CUI [1,3]
C1272705
pregnant woman
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
patient which may not cooperate to study procedures as evaluated by investigator
Descripción

Protocol Compliance Lacking

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C0332268
legally protected adult patient or patient unable to give an informed consent
Descripción

Protection of patient Legal | Informed Consent Unable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0412786
UMLS CUI [1,2]
C1301860
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
patient enrolled in an other clinical trial
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
patient which does not benefit from a social protection system
Descripción

Social Protection Benefit Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0242457
UMLS CUI [1,2]
C0814225
UMLS CUI [1,3]
C0332197
Renal Insufficiency
Descripción

Renal Insufficiency

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1565489
patient registered on a heart transplant waiting list
Descripción

Patient on waiting list Heart Transplantation

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0422768
UMLS CUI [1,2]
C0018823
disease and/or health condition which may interfere with study results
Descripción

Disease Interferes with Research results | Health condition Interferes with Research results

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0683954
UMLS CUI [2,1]
C2707304
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0683954
Volver a la parte superior de la página

Similar models

Eligibility Heart Failure NCT00887237

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
Age
Item
> 18 years old
boolean
C0001779 (UMLS CUI [1])
Indication Cardiac Resynchronization Therapy | New York Heart Association Classification
Item
cardiac resynchronization indication : new york heart association (nyha) class iii/iv
boolean
C3146298 (UMLS CUI [1,1])
C1167956 (UMLS CUI [1,2])
C1275491 (UMLS CUI [2])
QRS complex duration | New York Heart Association Classification
Item
& qrs width > 120 ms milliseconds (ms) or nyha class ii & qrs width > 150 ms
boolean
C0429025 (UMLS CUI [1])
C1275491 (UMLS CUI [2])
Sinus rhythm
Item
sinus rhythm
boolean
C0232201 (UMLS CUI [1])
Implantation procedure First
Item
first implant procedure
boolean
C0021107 (UMLS CUI [1,1])
C0205435 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Ventricular Tachycardia Permanent
Item
permanent ventricular tachycardia
boolean
C0042514 (UMLS CUI [1,1])
C0205355 (UMLS CUI [1,2])
Indication Pacing Permanent | Complete atrioventricular block
Item
permanent pacing indication for 3rd degree atrioventricular (av) block
boolean
C3146298 (UMLS CUI [1,1])
C0199640 (UMLS CUI [1,2])
C0205355 (UMLS CUI [1,3])
C0151517 (UMLS CUI [2])
Myocarditis | Myocarditis Suspected
Item
diagnosed or suspected acute myocarditis
boolean
C0027059 (UMLS CUI [1])
C0027059 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
Life Expectancy Due to Disease | Exception Cardiovascular Diseases
Item
less than 1 year life expectancy related to a non-cardiovascular disease
boolean
C0023671 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,3])
C1705847 (UMLS CUI [2,1])
C0007222 (UMLS CUI [2,2])
Clinical Study Follow-up Perform Unsuccessful
Item
impossibility to perform follow-up in the investigative center
boolean
C3274571 (UMLS CUI [1,1])
C0884358 (UMLS CUI [1,2])
C1272705 (UMLS CUI [1,3])
Pregnancy
Item
pregnant woman
boolean
C0032961 (UMLS CUI [1])
Protocol Compliance Lacking
Item
patient which may not cooperate to study procedures as evaluated by investigator
boolean
C0525058 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Protection of patient Legal | Informed Consent Unable
Item
legally protected adult patient or patient unable to give an informed consent
boolean
C0412786 (UMLS CUI [1,1])
C1301860 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Study Subject Participation Status
Item
patient enrolled in an other clinical trial
boolean
C2348568 (UMLS CUI [1])
Social Protection Benefit Absent
Item
patient which does not benefit from a social protection system
boolean
C0242457 (UMLS CUI [1,1])
C0814225 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Renal Insufficiency
Item
Renal Insufficiency
boolean
C1565489 (UMLS CUI [1])
Patient on waiting list Heart Transplantation
Item
patient registered on a heart transplant waiting list
boolean
C0422768 (UMLS CUI [1,1])
C0018823 (UMLS CUI [1,2])
Disease Interferes with Research results | Health condition Interferes with Research results
Item
disease and/or health condition which may interfere with study results
boolean
C0012634 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0683954 (UMLS CUI [1,3])
C2707304 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0683954 (UMLS CUI [2,3])
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