ID

36133

Descripción

Effect of Renal Denervation in End Staged Renal Disease With Resistant Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT02346045

Link

https://clinicaltrials.gov/show/NCT02346045

Palabras clave

Versiones (1)
  1. 17/4/19 17/4/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

17 de abril 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 Hypertension NCT02346045

Inglés

Eligibility Hypertension NCT02346045

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients who are under hemodialysis due to end stage renal disease
Descripción

Hemodialysis Due to End stage renal disease

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0019004
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0022661
patients who have resistant hypertension with office sbp >160 mmhg)
Descripción

HYPERTENSION RESISTANT | Systolic Pressure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0745130
UMLS CUI [2]
C0871470
patients who are or over 18 years old.
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
patients who submit informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
known secondary hypertension patients
Descripción

Secondary hypertension

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0155616
patients who have renal artery which is not adequate for renal denervation
Descripción

Renal artery Inadequate Renal artery denervation

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0035065
UMLS CUI [1,2]
C0205412
UMLS CUI [1,3]
C3544270
1. the main renal artery diameter < 4 mm, or renal artery length < 20 mm
Descripción

Renal artery Main Diameter | Renal artery Length

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0035065
UMLS CUI [1,2]
C1542147
UMLS CUI [1,3]
C1301886
UMLS CUI [2,1]
C0035065
UMLS CUI [2,2]
C1444754
2. the renal arteries into which stable catheter insertion is difficulty and which have hemodynamically or anatomically significant stenosis
Descripción

Structure of renal artery Catheterization Difficult | Renal Artery Stenosis

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0035065
UMLS CUI [1,2]
C0007430
UMLS CUI [1,3]
C0332218
UMLS CUI [2]
C0035067
3. the renal arteries who have undergone renal angioplasty
Descripción

Renal arteries Angioplasty

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0035065
UMLS CUI [1,2]
C1282893
patients who have history of myocardial infarction, unstable angina, syncope cerebrovascular insufficiency or extensive atherosclerotic disease with intravascular thrombosis, or unstable plaque
Descripción

Myocardial Infarction | Angina, Unstable | Syncope | Cerebrovascular Insufficiency | Atherosclerosis Extensive | Intravascular thrombosis | Plaque Unstable

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0002965
UMLS CUI [3]
C0039070
UMLS CUI [4]
C0241832
UMLS CUI [5,1]
C0004153
UMLS CUI [5,2]
C0205231
UMLS CUI [6]
C0442860
UMLS CUI [7,1]
C2936350
UMLS CUI [7,2]
C0443343
type 1 diabetes
Descripción

Diabetes Mellitus, Insulin-Dependent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011854
patients who have scheduled percutaneous coronary intervention (pci) or operation within 6 months
Descripción

Percutaneous Coronary Intervention Scheduled | Operative Surgical Procedures Scheduled

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0205539
UMLS CUI [2,1]
C0543467
UMLS CUI [2,2]
C0205539
hemodynamically significant valvular heart disease in which blood pressure reduction may cause significant deterioration of patient's health.
Descripción

Heart valve disease | Blood Pressure Reduction Causing Deteriorating condition of patient

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0018824
UMLS CUI [2,1]
C0005823
UMLS CUI [2,2]
C0392756
UMLS CUI [2,3]
C0678227
UMLS CUI [2,4]
C0555790
primary pulmonary hypertension
Descripción

Primary pulmonary hypertension

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0152171
patients who have the intracardiac defibrillator(icd) or pacemaker which do not allow delivery of radiofrequency energy.
Descripción

ICD | Artificial cardiac pacemaker

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0162589
UMLS CUI [2]
C0030163
patients who require continuous oxygen supply or mechanical ventilation for treatment of obstructive sleep apnea
Descripción

Oxygen supplementation Obstructive Sleep Apnea | Mechanical ventilation Obstructive Sleep Apnea

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0919655
UMLS CUI [1,2]
C0520679
UMLS CUI [2,1]
C0199470
UMLS CUI [2,2]
C0520679
patients who have serious medical condition which can compromise the safety of the patients and the safety and integrity of the study.
Descripción

Medical condition Serious compromises Patient safety | Medical condition compromises Integrity Clinical Trial

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C2945640
UMLS CUI [1,4]
C1113679
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C2945640
UMLS CUI [2,3]
C1947912
UMLS CUI [2,4]
C0008976
patients who have unresolved drug issue, alcoholism
Descripción

Drug use issue | Alcoholic Intoxication, Chronic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C4049580
UMLS CUI [2]
C0001973
patients who lack ability to understand and follow the instruction the researcher
Descripción

Protocol Compliance Unable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C1299582
patient who cannot follow up
Descripción

Follow-up Unable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C1299582
patients who are registered in other trial
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
patients who are pregnant, nursing or planning to be pregnant
Descripción

Pregnancy | Breast Feeding | Pregnancy, Planned

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032992
Volver a la parte superior de la página

Similar models

Eligibility Hypertension NCT02346045

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Hemodialysis Due to End stage renal disease
Item
patients who are under hemodialysis due to end stage renal disease
boolean
C0019004 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0022661 (UMLS CUI [1,3])
HYPERTENSION RESISTANT | Systolic Pressure
Item
patients who have resistant hypertension with office sbp >160 mmhg)
boolean
C0745130 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
Age
Item
patients who are or over 18 years old.
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
patients who submit informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Secondary hypertension
Item
known secondary hypertension patients
boolean
C0155616 (UMLS CUI [1])
Renal artery Inadequate Renal artery denervation
Item
patients who have renal artery which is not adequate for renal denervation
boolean
C0035065 (UMLS CUI [1,1])
C0205412 (UMLS CUI [1,2])
C3544270 (UMLS CUI [1,3])
Renal artery Main Diameter | Renal artery Length
Item
1. the main renal artery diameter < 4 mm, or renal artery length < 20 mm
boolean
C0035065 (UMLS CUI [1,1])
C1542147 (UMLS CUI [1,2])
C1301886 (UMLS CUI [1,3])
C0035065 (UMLS CUI [2,1])
C1444754 (UMLS CUI [2,2])
Structure of renal artery Catheterization Difficult | Renal Artery Stenosis
Item
2. the renal arteries into which stable catheter insertion is difficulty and which have hemodynamically or anatomically significant stenosis
boolean
C0035065 (UMLS CUI [1,1])
C0007430 (UMLS CUI [1,2])
C0332218 (UMLS CUI [1,3])
C0035067 (UMLS CUI [2])
Renal arteries Angioplasty
Item
3. the renal arteries who have undergone renal angioplasty
boolean
C0035065 (UMLS CUI [1,1])
C1282893 (UMLS CUI [1,2])
Myocardial Infarction | Angina, Unstable | Syncope | Cerebrovascular Insufficiency | Atherosclerosis Extensive | Intravascular thrombosis | Plaque Unstable
Item
patients who have history of myocardial infarction, unstable angina, syncope cerebrovascular insufficiency or extensive atherosclerotic disease with intravascular thrombosis, or unstable plaque
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0039070 (UMLS CUI [3])
C0241832 (UMLS CUI [4])
C0004153 (UMLS CUI [5,1])
C0205231 (UMLS CUI [5,2])
C0442860 (UMLS CUI [6])
C2936350 (UMLS CUI [7,1])
C0443343 (UMLS CUI [7,2])
Diabetes Mellitus, Insulin-Dependent
Item
type 1 diabetes
boolean
C0011854 (UMLS CUI [1])
Percutaneous Coronary Intervention Scheduled | Operative Surgical Procedures Scheduled
Item
patients who have scheduled percutaneous coronary intervention (pci) or operation within 6 months
boolean
C1532338 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
C0543467 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
Heart valve disease | Blood Pressure Reduction Causing Deteriorating condition of patient
Item
hemodynamically significant valvular heart disease in which blood pressure reduction may cause significant deterioration of patient's health.
boolean
C0018824 (UMLS CUI [1])
C0005823 (UMLS CUI [2,1])
C0392756 (UMLS CUI [2,2])
C0678227 (UMLS CUI [2,3])
C0555790 (UMLS CUI [2,4])
Primary pulmonary hypertension
Item
primary pulmonary hypertension
boolean
C0152171 (UMLS CUI [1])
ICD | Artificial cardiac pacemaker
Item
patients who have the intracardiac defibrillator(icd) or pacemaker which do not allow delivery of radiofrequency energy.
boolean
C0162589 (UMLS CUI [1])
C0030163 (UMLS CUI [2])
Oxygen supplementation Obstructive Sleep Apnea | Mechanical ventilation Obstructive Sleep Apnea
Item
patients who require continuous oxygen supply or mechanical ventilation for treatment of obstructive sleep apnea
boolean
C0919655 (UMLS CUI [1,1])
C0520679 (UMLS CUI [1,2])
C0199470 (UMLS CUI [2,1])
C0520679 (UMLS CUI [2,2])
Medical condition Serious compromises Patient safety | Medical condition compromises Integrity Clinical Trial
Item
patients who have serious medical condition which can compromise the safety of the patients and the safety and integrity of the study.
boolean
C3843040 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C2945640 (UMLS CUI [1,3])
C1113679 (UMLS CUI [1,4])
C3843040 (UMLS CUI [2,1])
C2945640 (UMLS CUI [2,2])
C1947912 (UMLS CUI [2,3])
C0008976 (UMLS CUI [2,4])
Drug use issue | Alcoholic Intoxication, Chronic
Item
patients who have unresolved drug issue, alcoholism
boolean
C4049580 (UMLS CUI [1])
C0001973 (UMLS CUI [2])
Protocol Compliance Unable
Item
patients who lack ability to understand and follow the instruction the researcher
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Follow-up Unable
Item
patient who cannot follow up
boolean
C3274571 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Study Subject Participation Status
Item
patients who are registered in other trial
boolean
C2348568 (UMLS CUI [1])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
patients who are pregnant, nursing or planning to be pregnant
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [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