ID

40825

Descripción

Randomized Controlled Trial of Lipid Apheresis in Patients With Elevated Lipoprotein(a); ODM derived from: https://clinicaltrials.gov/show/NCT01064934

Link

https://clinicaltrials.gov/show/NCT01064934

Palabras clave

Versiones (1)
  1. 19/5/20 19/5/20 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

19 de mayo de 2020

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 Hyperlipoproteinemia(a) NCT01064934

Inglés

Eligibility Hyperlipoproteinemia(a) NCT01064934

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
above 18 years of age
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
male or female
Descripción

Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
written informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
lipoprotein(a) >=60 mg/dl
Descripción

Lipoprotein (a) measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1096202
low-density lipoprotein cholesterol <130 mg/dl
Descripción

Low density lipoprotein cholesterol measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0202117
progressive cardiovascular disease
Descripción

Cardiovascular Disease Progressive

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0007222
UMLS CUI [1,2]
C0205329
positive recommendation by the inclusion committee
Descripción

Recommendation Positive

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0034866
UMLS CUI [1,2]
C1514241
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
current participation in a lipid apheresis program
Descripción

Participation Lipid Apheresis Program

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C0023779
UMLS CUI [1,3]
C0005791
UMLS CUI [1,4]
C3484370
previous participation in a lipid apheresis program
Descripción

Lipid Apheresis Program | Participation Previous

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0023779
UMLS CUI [1,2]
C0005791
UMLS CUI [1,3]
C3484370
UMLS CUI [2,1]
C0679823
UMLS CUI [2,2]
C0205156
low-density lipoprotein cholesterol >=130 mg/dl under maximally tolerated (or necessary) drug treatment
Descripción

Low density lipoprotein cholesterol measurement | Pharmacotherapy Maximum Tolerated Dose

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0202117
UMLS CUI [2,1]
C0013216
UMLS CUI [2,2]
C0752079
triglyceride concentrations >=450 mg/dl
Descripción

Triglycerides measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0202236
known homozygous familial hypercholesterolemia
Descripción

Familial hypercholesterolemia - homozygous

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0342881
known type iii hyperlipoproteinemia
Descripción

Hyperlipoproteinemia Type

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020476
UMLS CUI [1,2]
C0332307
pregnancy, breast feeding
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
history of malignant disease (with the exception of non-melanoma carcinomas of the skin and carcinoma in situ of the cervix)
Descripción

Malignant disease | Exception Skin carcinoma | Exception Carcinoma in situ of uterine cervix

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0442867
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0699893
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0851140
planned major surgical procedures in the next 3 months
Descripción

Major surgery Planned

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0679637
UMLS CUI [1,2]
C1301732
current participation in another interventional trial
Descripción

Study Subject Participation Status | Interventional Study

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C3274035
previous randomization in the current trial (applies only for the rct)
Descripción

Study Subject Participation Status | Randomization Previous

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0034656
UMLS CUI [2,2]
C0205156
Volver a la parte superior de la página

Similar models

Eligibility Hyperlipoproteinemia(a) NCT01064934

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
above 18 years of age
boolean
C0001779 (UMLS CUI [1])
Gender
Item
male or female
boolean
C0079399 (UMLS CUI [1])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Lipoprotein (a) measurement
Item
lipoprotein(a) >=60 mg/dl
boolean
C1096202 (UMLS CUI [1])
Low density lipoprotein cholesterol measurement
Item
low-density lipoprotein cholesterol <130 mg/dl
boolean
C0202117 (UMLS CUI [1])
Cardiovascular Disease Progressive
Item
progressive cardiovascular disease
boolean
C0007222 (UMLS CUI [1,1])
C0205329 (UMLS CUI [1,2])
Recommendation Positive
Item
positive recommendation by the inclusion committee
boolean
C0034866 (UMLS CUI [1,1])
C1514241 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Participation Lipid Apheresis Program
Item
current participation in a lipid apheresis program
boolean
C0679823 (UMLS CUI [1,1])
C0023779 (UMLS CUI [1,2])
C0005791 (UMLS CUI [1,3])
C3484370 (UMLS CUI [1,4])
Lipid Apheresis Program | Participation Previous
Item
previous participation in a lipid apheresis program
boolean
C0023779 (UMLS CUI [1,1])
C0005791 (UMLS CUI [1,2])
C3484370 (UMLS CUI [1,3])
C0679823 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
Low density lipoprotein cholesterol measurement | Pharmacotherapy Maximum Tolerated Dose
Item
low-density lipoprotein cholesterol >=130 mg/dl under maximally tolerated (or necessary) drug treatment
boolean
C0202117 (UMLS CUI [1])
C0013216 (UMLS CUI [2,1])
C0752079 (UMLS CUI [2,2])
Triglycerides measurement
Item
triglyceride concentrations >=450 mg/dl
boolean
C0202236 (UMLS CUI [1])
Familial hypercholesterolemia - homozygous
Item
known homozygous familial hypercholesterolemia
boolean
C0342881 (UMLS CUI [1])
Hyperlipoproteinemia Type
Item
known type iii hyperlipoproteinemia
boolean
C0020476 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnancy, breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Malignant disease | Exception Skin carcinoma | Exception Carcinoma in situ of uterine cervix
Item
history of malignant disease (with the exception of non-melanoma carcinomas of the skin and carcinoma in situ of the cervix)
boolean
C0442867 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0699893 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0851140 (UMLS CUI [3,2])
Major surgery Planned
Item
planned major surgical procedures in the next 3 months
boolean
C0679637 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
Study Subject Participation Status | Interventional Study
Item
current participation in another interventional trial
boolean
C2348568 (UMLS CUI [1])
C3274035 (UMLS CUI [2])
Study Subject Participation Status | Randomization Previous
Item
previous randomization in the current trial (applies only for the rct)
boolean
C2348568 (UMLS CUI [1])
C0034656 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
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