ID

17170

Descripción

Open Label High Dose Ropinirole (Requip) Study for Patients With Parkinson's Disease; ODM derived from: https://clinicaltrials.gov/show/NCT00260793

Link

https://clinicaltrials.gov/show/NCT00260793

Palabras clave

  1. 29/8/16 29/8/16 -
Subido en

29 de agosto de 2016

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.

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 Parkinson's Disease NCT00260793

Eligibility Parkinson's Disease NCT00260793

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients must give written informed consent prior to any specific study procedures.
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
males or females; females of childbearing age who are not currently pregnant must agree to use a medically accepted method of contraception throughout the study.
Descripción

Contraception

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0700589
age greater than or equal to 25 years.
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
patients must be on a maximum dose of dopamine agonist drug (pergolide 4mg/day, pramipexole 4.5 mg/day or ropinirole 24mg/day).
Descripción

Maximum dose of dopamine agonist drug

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0178601
UMLS CUI [1,2]
C0178602
stable dose of all medications for 4 weeks.
Descripción

Stable dose of all medications

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0205360
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
current hallucinations.
Descripción

Hallucinations

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0018524
history of disabling hallucinations or hallucinations in past requiring treatment.
Descripción

Hallucinations requiring treatment

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018524
UMLS CUI [1,2]
C0087111
troublesome edema (swelling).
Descripción

Edema

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013604
unstable depression.
Descripción

Depression

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011570
female who is pregnant or lactating.
Descripción

pregnant or lactating

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
use of an investigational drug with in the last 30 days.
Descripción

Investigational drug

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013230
other inclusion or exclusion criteria to be evaluated by the physician.
Descripción

Other inclusion or exclusion criteria

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1516637

Similar models

Eligibility Parkinson's Disease NCT00260793

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
patients must give written informed consent prior to any specific study procedures.
boolean
C0021430 (UMLS CUI [1])
Contraception
Item
males or females; females of childbearing age who are not currently pregnant must agree to use a medically accepted method of contraception throughout the study.
boolean
C0700589 (UMLS CUI [1])
Age
Item
age greater than or equal to 25 years.
boolean
C0001779 (UMLS CUI [1])
Maximum dose of dopamine agonist drug
Item
patients must be on a maximum dose of dopamine agonist drug (pergolide 4mg/day, pramipexole 4.5 mg/day or ropinirole 24mg/day).
boolean
C0178601 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Stable dose of all medications
Item
stable dose of all medications for 4 weeks.
boolean
C0178602 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Hallucinations
Item
current hallucinations.
boolean
C0018524 (UMLS CUI [1])
Hallucinations requiring treatment
Item
history of disabling hallucinations or hallucinations in past requiring treatment.
boolean
C0018524 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Edema
Item
troublesome edema (swelling).
boolean
C0013604 (UMLS CUI [1])
Depression
Item
unstable depression.
boolean
C0011570 (UMLS CUI [1])
pregnant or lactating
Item
female who is pregnant or lactating.
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
Investigational drug
Item
use of an investigational drug with in the last 30 days.
boolean
C0013230 (UMLS CUI [1])
Other inclusion or exclusion criteria
Item
other inclusion or exclusion criteria to be evaluated by the physician.
boolean
C1516637 (UMLS CUI [1])

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

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